The following data is part of a premarket notification filed by Advanced Surgical Products, Inc. with the FDA for Prisma Disposable U-shaped Cannula.
Device ID | K874998 |
510k Number | K874998 |
Device Name: | PRISMA DISPOSABLE U-SHAPED CANNULA |
Classification | Cannula, Ophthalmic |
Applicant | ADVANCED SURGICAL PRODUCTS, INC. 744 GODDARD Chesterfield, MO 63017 |
Contact | Todd J Hessel |
Correspondent | Todd J Hessel ADVANCED SURGICAL PRODUCTS, INC. 744 GODDARD Chesterfield, MO 63017 |
Product Code | HMX |
CFR Regulation Number | 886.4350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-12-02 |
Decision Date | 1988-04-13 |