K. W. Griffen Co.
Norwalk, CT, US
K. W. GRIFFEN CO. appears in FDA device records in Norwalk, CT. FDA records list 4 510(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 4 510(k) clearances for K. W. Griffen Co. between 1987 and 1996. The busiest year on record is 1987, with 2. The most recent is 1996, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1987 | 2 |
| 1995 | 1 |
| 1996 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K961098 | BIO-DRESSING, STERILE ISLAND DRESSING | MGP | Substantially Equivalent for Some Indications | |
| K953810 | FLUFF GAUZE BANDAGE, STERILE & NON-STERILE | EFQ | Substantially Equivalent | |
| K874161 | MODIFIED USE OF TRIANGLE BANDAGE STERILE | NAD | Substantially Equivalent | |
| K870258 | BIOSCRUB SURGICAL SCRUB BRUSH | GEC | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1211177 | 1211177 | K. W. GRIFFEN CO. | 100 PEARL ST., NORWALK, CT 06850 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