The following data is part of a premarket notification filed by Optikos Shami, Inc. with the FDA for Optikos Shami, Inc. Spectacle Frames.
Device ID | K934198 |
510k Number | K934198 |
Device Name: | OPTIKOS SHAMI, INC. SPECTACLE FRAMES |
Classification | Frame, Spectacle |
Applicant | OPTIKOS SHAMI, INC. 15375 BARRANCA PKWY. STE. G106 Irvine, CA 92718 |
Contact | Ray Bilbessi |
Correspondent | Ray Bilbessi OPTIKOS SHAMI, INC. 15375 BARRANCA PKWY. STE. G106 Irvine, CA 92718 |
Product Code | HQZ |
CFR Regulation Number | 886.5842 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-08-26 |
Decision Date | 1993-10-04 |