The following data is part of a premarket notification filed by Kit Pak, Inc. with the FDA for Wound Dressing Kit.
Device ID | K923905 |
510k Number | K923905 |
Device Name: | WOUND DRESSING KIT |
Classification | Wound Dressing Kit |
Applicant | KIT PAK, INC. 825 CHASE AVE. Elk Grove Village, IL 60007 |
Contact | Thomas Sanders |
Correspondent | Thomas Sanders KIT PAK, INC. 825 CHASE AVE. Elk Grove Village, IL 60007 |
Product Code | MCY |
CFR Regulation Number | 880.5075 [🔎] |
Decision | Substantially Equivalent - Kit With Drugs (SEKD) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-08-04 |
Decision Date | 1993-07-02 |