510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K961512Substantially Equivalent

Perkins Hand-Held Applanation Tonometer

Clement Clarke, Inc., England, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K961512 is the FDA 510(k) clearance record for PERKINS HAND-HELD APPLANATION TONOMETER, a class II device, cleared for Clement Clarke, Inc. on under FDA product code HKY (Tonometer, Manual). FDA records list 10 510(k) clearances for Clement Clarke, Inc., from to . As of , FDA records show no recalls naming K961512.

Clearance record

Decision date
Received
(90 days to decision)
Product code
HKY Tonometer, Manual
Regulation
21 CFR 886.1930
Device class
Class II
Review panel
Ophthalmic
Applicant
Clement Clarke, Inc. Airmed House, Edinburgh Way, England, GB
510(k) summary
Statement
Third party review
No

Clearances, product code HKY

Trailing 12 months

FDA records hold no clearances under product code HKY in the trailing twelve months.

FDA records show no clearances under product code HKY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HKY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260