Kerma Medical Products, Inc.
Suffolk, VA, US
KERMA MEDICAL PRODUCTS, INC. appears in FDA device records in Suffolk, VA. FDA records list 5 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 5 510(k) clearances for Kerma Medical Products, Inc. between 1991 and 1994. The busiest year on record is 1991, with 2. The most recent is 1994, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1991 | 2 |
| 1992 | 2 |
| 1994 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K931042 | MOORE SECURE CAP | LYU | Substantially Equivalent | |
| K915821 | MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES | NAB | Substantially Equivalent | |
| K915822 | MULTIPLE DRESSING, STERILE NONADDHERENT PADS | NAB | Substantially Equivalent | |
| K914937 | STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES | NAB | Substantially Equivalent | |
| K914071 | MULTIPLE BURN DRESSING | NAB | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1123029 | 1000123280 | KERMA MEDICAL PRODUCTS, INC. | 215 Suburban Dr, Suffolk, VA 23434 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
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