510(k) K875107

HEALTH CARE EYE PROTECTION by Surgikos, Inc. — Product Code HOY

K875107 is an FDA 510(k) premarket notification submitted by Surgikos, Inc. for the device "HEALTH CARE EYE PROTECTION". The FDA issued a decision of Substantially Equivalent on March 21, 1988. 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. Surgikos, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 21, 1988
Date Received
December 14, 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