510(k) K872000
K872000 is an FDA 510(k) premarket notification submitted by Treace Medical, Inc. for the device "EYE GARD". The FDA issued a decision of Substantially Equivalent on July 21, 1987. The device falls under product code HOY (Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)), a Class I device regulated under 21 CFR 886.4750. Treace Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 21, 1987
- Date Received
- May 26, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- Device Class
- Class I
- Regulation Number
- 886.4750
- Review Panel
- OP
- Submission Type