The following data is part of a premarket notification filed by Procyte Corp. with the FDA for Osmocyte Wound Manager Sheet Dressing.
Device ID | K965143 |
510k Number | K965143 |
Device Name: | OSMOCYTE WOUND MANAGER SHEET DRESSING |
Classification | Dressing, Wound And Burn, Hydrogel W/drug And/or Biologic |
Applicant | PROCYTE CORP. 12040 115TH AVENUE NE SUITE 210 Kirkland, WA 98034 -6900 |
Contact | Paul Ketteridge |
Correspondent | Paul Ketteridge PROCYTE CORP. 12040 115TH AVENUE NE SUITE 210 Kirkland, WA 98034 -6900 |
Product Code | MGQ |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-12-23 |
Decision Date | 1997-05-22 |
Summary: | summary |