The following data is part of a premarket notification filed by Vitaphore Corp. with the FDA for Collagen Shield For Acute Care.
Device ID | K913148 |
510k Number | K913148 |
Device Name: | COLLAGEN SHIELD FOR ACUTE CARE |
Classification | Collagen Corneal Shield |
Applicant | VITAPHORE CORP. 1505 O'BRIEN DR. Menlo Park, CA 94025 |
Contact | Jan Tomsic |
Correspondent | Jan Tomsic VITAPHORE CORP. 1505 O'BRIEN DR. Menlo Park, CA 94025 |
Product Code | MOE |
CFR Regulation Number | 886.4750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-07-16 |
Decision Date | 1991-10-15 |