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

Device, Aversive Conditioning

21 CFR 882.5235 / Neurology
FDA source (opens on fda.gov)

HCB is the FDA product code for Device, Aversive Conditioning, a class II device type, regulated under 21 CFR 882.5235. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HCB
Device name
Device, Aversive Conditioning
Regulation
21 CFR 882.5235
Device class
Class II
Review panel
Neurology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
6
Ingested recalls
0

Clearances, product code HCB

By decision year
6 clearances under product code HCB with a decision year between 1976 and 1994, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HCB by decision year
YearClearances
19761
19791
19821
19861
19871
19941

Applicants with the most clearances

Product code HCB
Applicants holding the most 510(k) clearances under product code HCB
ApplicantClearances
Behavior Research Institute, Inc.1
Farrall Instruments, Inc.1
Human Technologies, Inc.1
Jackson Ent.1
Michael R. Kiss1
Oxford Medilog, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code