Microbio-Medics, Inc.
Columbus, MS, US
Microbio-Medics, Inc. appears in FDA device records in Columbus, MS. FDA records list 13 510(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
- 13
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 13 510(k) clearances for Microbio-Medics, Inc. between 1988 and 1993. The busiest year on record is 1989, with 4. The most recent is 1993, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 2 |
| 1989 | 4 |
| 1990 | 2 |
| 1991 | 3 |
| 1992 | 1 |
| 1993 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K923353 | VENTILATION TUBES W/ HYDROGEL COATING | ETD | Substantially Equivalent | |
| K922572 | 321Q MINIMUM ENERGY TINNITUS SUPPRESSOR | KLW | Substantially Equivalent | |
| K913276 | MICROTEK MEDICAL'S SOUND STIKS | EWO | Substantially Equivalent | |
| K904239 | SOFT HYDROXYLAPATITE OSSICULAR MALLEABLE PROSTHES | ETA | Substantially Equivalent | |
| K910167 | MICROTEK-HERITAGES SILICONE BULB EVACUATION SYSTEM | GCY | Substantially Equivalent | |
| K900726 | MICROTEK MEDICAL'S BLOOD COLLECTION KIT | JKA | Substantially Equivalent | |
| K901154 | MICROTEK'S SURGICAL LAMP HANDLE & COVER | FTA | Substantially Equivalent | |
| K895815 | MICROTEK TOTAL OSSICULAR PROTHESIS | ETA | Substantially Equivalent | |
| K895814 | MICROTEK PISTON & WIRE PROSTHESES | ETB | Substantially Equivalent | |
| K895502 | MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINT | EPP | Substantially Equivalent | |
| K885201 | OSSICULAR PROSTHESES 4 PARTIAL, 4 TOTAL, 2 CONVERT | ETA | Substantially Equivalent | |
| K882422 | DISPOSABLE ARACHNOID KNIFE | HAO | Substantially Equivalent | |
| K882724 | MICROTEK PROBE DRAPE | KKX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- GCYApparatus, Suction, Single Patient Use, Portable, Nonpowered
- EWOAudiometer
- KKXDrape, Surgical, Antimicrobial
- HAOInstrument, Surgical, Non-Powered
- FTALight, Surgical, Accessories
- KLWMasker, Tinnitus
- ETBProsthesis, Partial Ossicular Replacement
- ETAReplacement, Ossicular Prosthesis, Total
- EPPSplint, Nasal
- ETDTube, Tympanostomy
- JKATubes, Vials, Systems, Serum Separators, Blood Collection
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