Matrix Medica, Inc.
Minden, NV, US
Matrix Medica, Inc. appears in FDA device records in Minden, NV. FDA records list 14 510(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
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Matrix Medica, Inc. between 1985 and 1996. The busiest year on record is 1989, with 3. The most recent is 1996, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 2 |
| 1987 | 1 |
| 1989 | 3 |
| 1990 | 3 |
| 1991 | 2 |
| 1994 | 1 |
| 1996 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K961536 | FLEXSCOPE | GDB | Substantially Equivalent | |
| K923693 | KLORMAN | LRJ | Substantially Equivalent | |
| K921982 | MATRX HOPE(R) 5 RESUSCITATOR | BTM | Substantially Equivalent | |
| K915353 | MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP | EIA | Substantially Equivalent | |
| K912661 | MATRX, PYRAMID TRIANGLE BANDAGE | ILI | Substantially Equivalent | |
| K900551 | MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC. | DRS | Substantially Equivalent | |
| K895533 | LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER | LDD | Substantially Equivalent | |
| K895525 | MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER | DRL | Substantially Equivalent | |
| K893219 | MATRX DENTAL UNIT | EIA | Substantially Equivalent | |
| K883833 | NITRONOX(R), FIRST RESPONSE NITRONOX(TM) | BZR | Substantially Equivalent | |
| K884879 | CENTURION(TM) MIXER | BSZ | Substantially Equivalent | |
| K873277 | MITRAFLEX(TM) WOUND DRESSING | NAD | Substantially Equivalent for Some Indications | |
| K850661 | MATRIX DRI-IDEA BOOTIES | Substantially Equivalent | ||
| K850177 | MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN) | FYA | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- LDDDc-Defibrillator, Low-Energy, (Including Paddles)
- LRJDisinfectant, Medical Devices
- NADDressing, Wound, Occlusive
- GDBEndoscope, Fiber Optic
- BSZGas-Machine, Anesthesia
- FYAGown, Surgical
- BZRMixer, Breathing Gases, Anesthesia Inhalation
- ILISling, Arm
- DRLTester, Defibrillator
- DRSTransducer, Blood-Pressure, Extravascular
- EIAUnit, Operative Dental
- BTMVentilator, Emergency, Manual (Resuscitator)
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain