Medical Device Manufacturer · US , Kirkland , WA

Procyte Corp. - FDA 510(k) Cleared Devices

9 submissions · 5 cleared · Since 1996

Total

Cleared

Denied

Procyte Corp. has 5 FDA 510(k) cleared medical devices. Based in Kirkland, US.

Historical record: 5 cleared submissions from 1996 to 1998. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Procyte Corp. Filter by specialty or product code using the sidebar.

Procyte Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Procyte Corp.

9 devices

1-9 of 9

Cleared Mar 16, 1998

OSMO/PCA PILLOW WOUND DRESSING

K971612 · KMF

General & Plastic Surgery · 318d

Cleared Dec 10, 1997

OSMOCYTE ISLAND WOUND DRESSING

K972150 · KMF

General & Plastic Surgery · 184d

Cleared Dec 10, 1997

OSMOCYTE RA WOUND DRESSING

K972329 · KMF

General & Plastic Surgery · 170d

Cleared Jun 05, 1997

LAMIN-2 HYDRATING GEL

K970153 · MGQ

General & Plastic Surgery · 140d

Cleared May 22, 1997

OSMOCYTE WOUND MANAGER SHEET DRESSING

K965143 · MGQ

General & Plastic Surgery · 150d

Cleared Feb 24, 1997

IAMIN IMPREGNATED GAUZE DRESSING

K965005 · MGQ

General & Plastic Surgery · 70d

Cleared Feb 03, 1997

IAMIN WET DRESSING (COPPER-SALINE)

K964468 · MGQ

General & Plastic Surgery · 89d

Cleared Nov 26, 1996

OSMOCYTE ULTRA/PE PILLOW WOUND DRESSING

K962623 · KMF

General & Plastic Surgery · 144d

Cleared Feb 05, 1996

IAMIN GEL WOUND DRESSING

K953853 · MGQ

General & Plastic Surgery · 173d

Procyte Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Procyte Corp.

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