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

Rack, Clip

21 CFR 882.4215 / Neurology
FDA source (opens on fda.gov)

HBR is the FDA product code for Rack, Clip, a class I device type, regulated under 21 CFR 882.4215. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
HBR
Device name
Rack, Clip
Regulation
21 CFR 882.4215
Device class
Class I
Review panel
Neurology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code HBR

By decision year
1 clearance under product code HBR with a decision year between 1989 and 1989, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HBR by decision year
YearClearances
19891

Applicants with the most clearances

Product code HBR
Applicants holding the most 510(k) clearances under product code HBR
ApplicantClearances
Kinetic Medical Products1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 16 companies shown, in name order