510(k) K841762

WOODLYN APPLANATION TONOMETER by Woodlyn, Inc. — Product Code HKX

K841762 is an FDA 510(k) premarket notification submitted by Woodlyn, Inc. for the device "WOODLYN APPLANATION TONOMETER". The FDA issued a decision of Substantially Equivalent on August 2, 1984. The device falls under product code HKX (Tonometer, Ac-Powered), a Class II device regulated under 21 CFR 886.1930. Woodlyn, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 2, 1984
Date Received
April 27, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tonometer, Ac-Powered
Device Class
Class II
Regulation Number
886.1930
Review Panel
OP
Submission Type