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

Esthesiometer, Ocular

21 CFR 886.1040 / Ophthalmic
FDA source (opens on fda.gov)

HJC is the FDA product code for Esthesiometer, Ocular, a class I device type, regulated under 21 CFR 886.1040. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HJC
Device name
Esthesiometer, Ocular
Regulation
21 CFR 886.1040
Device class
Class I
Review panel
Ophthalmic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code HJC

By decision year
2 clearances under product code HJC with a decision year between 1985 and 1992, 1985 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HJC by decision year
YearClearances
19851
19921

Applicants with the most clearances

Product code HJC
Applicants holding the most 510(k) clearances under product code HJC
ApplicantClearances
Connecticut Bioinstruments, Inc.1
Luneau SA1

Companies listing this code with FDA

Companies whose registered establishments list this code