510(k) K770041

SCISSORS, STRABISMUS, 4 CURVED by J. Sklar Mfg. Co., Inc. — Product Code HNF

K770041 is an FDA 510(k) premarket notification submitted by J. Sklar Mfg. Co., Inc. for the device "SCISSORS, STRABISMUS, 4 CURVED". The FDA issued a decision of Substantially Equivalent on January 14, 1977. The device falls under product code HNF (Scissors, Ophthalmic), a Class I device regulated under 21 CFR 886.4350. J. Sklar Mfg. Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 14, 1977
Date Received
January 10, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Scissors, Ophthalmic
Device Class
Class I
Regulation Number
886.4350
Review Panel
OP
Submission Type