510(k) K870440

LOOK LENS LOOPS by Look, Inc. — Product Code HNQ

K870440 is an FDA 510(k) premarket notification submitted by Look, Inc. for the device "LOOK LENS LOOPS". The FDA issued a decision of Substantially Equivalent on February 20, 1987. The device falls under product code HNQ (Hook, Ophthalmic), a Class I device regulated under 21 CFR 886.4350. Look, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 20, 1987
Date Received
February 3, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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