The following data is part of a premarket notification filed by Cook Biotech, Inc. with the FDA for Sis Wound Dressing Ii.
Device ID | K993948 |
510k Number | K993948 |
Device Name: | SIS WOUND DRESSING II |
Classification | Dressing, Wound, Collagen |
Applicant | COOK BIOTECH, INC. 3055 KENT AVE. West Lafayette, IN 47906 -1076 |
Contact | Neal E Fearnot |
Correspondent | Neal E Fearnot COOK BIOTECH, INC. 3055 KENT AVE. West Lafayette, IN 47906 -1076 |
Product Code | KGN |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-11-22 |
Decision Date | 2000-01-06 |
Summary: | summary |