510(k) K012096
K012096 is an FDA 510(k) premarket notification submitted by Ocular Instruments, Inc. for the device "DISPOSABLE VITRECTOMY LENS". The FDA issued a decision of Substantially Equivalent on August 24, 2001. 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
- August 24, 2001
- Date Received
- July 5, 2001
- 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