The following data is part of a premarket notification filed by O.r. Specialties, Inc. with the FDA for Disposable Scleral Plugs.
Device ID | K925671 |
510k Number | K925671 |
Device Name: | DISPOSABLE SCLERAL PLUGS |
Classification | Plug, Scleral |
Applicant | O.R. SPECIALTIES, INC. 4749 APPLETREE LN. Tuscaloosa, AL 35405 |
Contact | Jack W Howard |
Correspondent | Jack W Howard O.R. SPECIALTIES, INC. 4749 APPLETREE LN. Tuscaloosa, AL 35405 |
Product Code | LXP |
CFR Regulation Number | 886.4155 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-11-10 |
Decision Date | 1993-08-02 |