510(k) K933264
K933264 is an FDA 510(k) premarket notification submitted by Ocular Instruments, Inc. for the device "RITCH NYLON SUTURE LASER LENS". The FDA issued a decision of Substantially Equivalent on October 31, 1994. The device falls under product code HJK (Lens, Contact, Polymethylmethacrylate, Diagnostic), a Class II device regulated under 21 CFR 886.1385. Ocular Instruments, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 31, 1994
- Date Received
- July 6, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lens, Contact, Polymethylmethacrylate, Diagnostic
- Device Class
- Class II
- Regulation Number
- 886.1385
- Review Panel
- OP
- Submission Type