Procyte Corp.
Kirkland, WA, US
Procyte Corp. appears in FDA device records in Kirkland, WA. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Procyte Corp. between 1996 and 1998. The busiest year on record is 1997, with 6. The most recent is 1998, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1996 | 2 |
| 1997 | 6 |
| 1998 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K971612 | OSMO/PCA PILLOW WOUND DRESSING | KMF | Substantially Equivalent for Some Indications | |
| K972329 | OSMOCYTE RA WOUND DRESSING | KMF | Substantially Equivalent for Some Indications | |
| K972150 | OSMOCYTE ISLAND WOUND DRESSING | KMF | Substantially Equivalent for Some Indications | |
| K970153 | LAMIN-2 HYDRATING GEL | MGQ | Substantially Equivalent | |
| K965143 | OSMOCYTE WOUND MANAGER SHEET DRESSING | MGQ | Substantially Equivalent | |
| K965005 | IAMIN IMPREGNATED GAUZE DRESSING | MGQ | Substantially Equivalent | |
| K964468 | IAMIN WET DRESSING (COPPER-SALINE) | MGQ | Substantially Equivalent | |
| K962623 | OSMOCYTE ULTRA/PE PILLOW WOUND DRESSING | KMF | Substantially Equivalent | |
| K953853 | IAMIN GEL WOUND DRESSING | MGQ | Substantially Equivalent for Some Indications |
Registered establishments
No FDA establishment registrations recorded against this company.
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