510(k) K875014
K875014 is an FDA 510(k) premarket notification submitted by Labtician Products, Inc. for the device "LABTICIAN RETINAL IMPLANTS". The FDA issued a decision of Substantially Equivalent on February 26, 1988. The device falls under product code HQJ (Implant, Absorbable, (Scleral Buckling Methods)), a Class II device regulated under 21 CFR 886.3300.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 26, 1988
- Date Received
- December 4, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Implant, Absorbable, (Scleral Buckling Methods)
- Device Class
- Class II
- Regulation Number
- 886.3300
- Review Panel
- OP
- Submission Type