The following data is part of a premarket notification filed by Advanced Surgical Products, Inc. with the FDA for Prisma Disposable 19 And 20 Gauge Scleral Plugs.
Device ID | K880952 |
510k Number | K880952 |
Device Name: | PRISMA DISPOSABLE 19 AND 20 GAUGE SCLERAL PLUGS |
Classification | Plug, Scleral |
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 | LXP |
CFR Regulation Number | 886.4155 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-03-07 |
Decision Date | 1988-05-13 |