Burron Medical Products, Inc.
Mchenry, IL, US
Burron Medical Products, Inc. appears in FDA device records in Mchenry, IL. FDA records list 41 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 41
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 41 510(k) clearances for Burron Medical Products, Inc. between 1979 and 1987. The busiest year on record is 1981, with 13. The most recent is 1987, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1980 | 7 |
| 1981 | 13 |
| 1982 | 6 |
| 1983 | 3 |
| 1984 | 6 |
| 1986 | 4 |
| 1987 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K870403 | CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTURE | FOZ | Substantially Equivalent | |
| K862412 | INTESTOPLANT | LLD | Substantially Equivalent | |
| K861479 | CAVAFIX, CENTRAL VENOUS CATHETER KIT | FOZ | Unknown | |
| K860126 | STIMUPLEX, NERVE STIMULATOR | BXN | Substantially Equivalent | |
| K851293 | IMPLANTOFIX | LJT | Substantially Equivalent | |
| K841428 | JEJUNOSTOMY SET FOR TUBE FEEDING | KNT | Substantially Equivalent | |
| K834383 | DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT | LJS | Substantially Equivalent | |
| K834299 | LONG TERM CENTRAL VENOUS ACCESS CATH | LJS | Substantially Equivalent | |
| K834473 | MULTI-LUMEN CENTRAL VENOUS CATH. KIT | LJS | Substantially Equivalent | |
| K840179 | CONTINUOUS EPIDURAL ANESTHES. TRAY | CAZ | Substantially Equivalent | |
| K840287 | BRACHIAL PLEXUS ANESTHESIA TRAY | CAZ | Substantially Equivalent | |
| K830571 | BOTTLE ADAPTER | KYX | Substantially Equivalent | |
| K830572 | CLEAN-FLUSH | KYZ | Substantially Equivalent | |
| K830193 | CAT 3040 | KPE | Substantially Equivalent | |
| K820454 | THE RED CAP | FMF | Substantially Equivalent | |
| K820453 | THE INT-STOPPER | FPA | Substantially Equivalent | |
| K820004 | PLEUROFIX THORACENTESIS KIT | GAZ | Substantially Equivalent | |
| K820047 | SPINOCAN SPINAL NEEDLE | BSP | Substantially Equivalent | |
| K813396 | VERSCHLUBSTOPFEN COMB-CLOSING STOPPER | FOZ | Substantially Equivalent | |
| K813498 | MEDIFIX | KRK | Substantially Equivalent | |
| K813259 | IN-STOPPER (INJECTION CAP | FPA | Substantially Equivalent | |
| K813084 | CYSTOFIX SUPRAPUBIC BLADDER DRAIN SET | KOB | Substantially Equivalent | |
| K813082 | UREOFIX 500 URINE MEASURING SYSTEM | FFG | Substantially Equivalent | |
| K813195 | MEDIFIX GRADUATED SCALE | KRK | Substantially Equivalent | |
| K813081 | HISTOCAN BIOPSY NEEDLE | Substantially Equivalent | ||
| K813236 | EPICAN EPIDURAL CANNULA, BEVEL ACCORD | BSP | Substantially Equivalent | |
| K813186 | PERFIX SET FOR EPIDURAL ANESTHESIA W/TUO | CAZ | Substantially Equivalent | |
| K813179 | PERICAN, EPIDURAL CANNULA | BSP | Substantially Equivalent | |
| K813165 | PLEXUFIX BRACHIAL PLEXUS ANESTH. NEEDLE | BSP | Substantially Equivalent | |
| K813085 | HEPAFIX BIOPSY NEEDLE SET | KNW | Substantially Equivalent | |
| K813083 | VENOFIX SCALP VEIN SET | FPA | Substantially Equivalent | |
| K810461 | BURRON CENTRAL VEIN CATHERIZATION KIT | DQY | Substantially Equivalent | |
| K810460 | BURRON PERCUTANEOUS INDUCER SET | DQY | Substantially Equivalent | |
| K801941 | BURRON MICROCATH INTRA. CATH. PLACEMENTT | FOZ | Substantially Equivalent | |
| K801605 | BIMECO FILTERED EXTENSION SET | FPB | Substantially Equivalent | |
| K801311 | BURRON MULTI-AD SYRINGE CAP | FMF | Substantially Equivalent | |
| K801008 | MULTI-AD FLUID DISPENSING PUMP MP-3000 | KYX | Substantially Equivalent | |
| K801108 | DOUBLE ENDED VENTED TRANSFER DEVICE | FMI | Substantially Equivalent | |
| K801107 | DOUBLE ENDED FILTERED TRANSFER NEEDLE | FMI | Substantially Equivalent | |
| K800437 | SYRINGE TIP CONNECTOR | KYX | Substantially Equivalent | |
| K791020 | FLUID ADMINISTRATION SET FA-3160 | EYN | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- CAZAnesthesia Conduction Kit
- LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- DQYCatheter, Percutaneous
- KOBCatheter, Suprapubic (And Accessories)
- KPEContainer, I.V.
- FFGDevice, Urine Flow Rate Measuring, Non-Electrical, Disposable
- KYXDispenser, Liquid Medication
- FPBFilter, Infusion Line
- KNWInstrument, Biopsy
- KRKManometer, Blood-Pressure, Venous
- BSPNeedle, Conduction, Anesthetic (W/Wo Introducer)
- FMINeedle, Hypodermic, Single Lumen
- LLDPort & Catheter, Implanted, Subcutaneous, Intraperitoneal
- LJTPort & Catheter, Implanted, Subcutaneous, Intravascular
- FPASet, Administration, Intravascular
- BXNStimulator, Nerve, Battery-Powered
- KYZSyringe, Irrigating (Non Dental)
- FMFSyringe, Piston
- EYNTray, Irrigation, Sterile
- KNTTubes, Gastrointestinal (And Accessories)
- GAZTubing, Noninvasive
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain