510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920271Substantially Equivalent

Weinstein Corneal Mircoaesthesiometer

Connecticut Bioinstruments, Inc., Danbury CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920271 is the FDA 510(k) clearance record for WEINSTEIN CORNEAL MIRCOAESTHESIOMETER, a class I device, cleared for Connecticut Bioinstruments, Inc. on under FDA product code HJC (Esthesiometer, Ocular). FDA records list one 510(k) clearance for Connecticut Bioinstruments, Inc. As of , FDA records show no recalls naming K920271.

Clearance record

Decision date
Received
(90 days to decision)
Product code
HJC Esthesiometer, Ocular
Regulation
21 CFR 886.1040
Device class
Class I
Review panel
Ophthalmic
Applicant
Connecticut Bioinstruments, Inc. 5 B Oak Ln., Danbury CT
510(k) summary
Statement
Third party review
No

Clearances, product code HJC

Trailing 12 months

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

FDA records show no clearances under product code HJC in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HJC, 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