The following data is part of a premarket notification filed by Gamp & Assoc. with the FDA for Gamp & Associates Disposable Fiberoptic Endoilluminator.
Device ID | K952586 |
510k Number | K952586 |
Device Name: | GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC ENDOILLUMINATOR |
Classification | Endoilluminator |
Applicant | GAMP & ASSOC. 3237 HAAS Bridgeton, MO 63044 |
Contact | James Taylor |
Correspondent | James Taylor GAMP & ASSOC. 3237 HAAS Bridgeton, MO 63044 |
Product Code | MPA |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-06-05 |
Decision Date | 1995-09-01 |