510(k) K770389

LENS SET, MENTOR TRIAL by Codman & Shurtleff, Inc. — Product Code HPC

K770389 is an FDA 510(k) premarket notification submitted by Codman & Shurtleff, Inc. for the device "LENS SET, MENTOR TRIAL". The FDA issued a decision of Substantially Equivalent on March 14, 1977. The device falls under product code HPC (Set, Lens, Trial, Ophthalmic), a Class I device regulated under 21 CFR 886.1405. Codman & Shurtleff, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 14, 1977
Date Received
February 28, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Lens, Trial, Ophthalmic
Device Class
Class I
Regulation Number
886.1405
Review Panel
OP
Submission Type