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

Bars, Parallel, Powered

21 CFR 890.5380 / Physical Medicine
FDA source (opens on fda.gov)

IRR is the FDA product code for Bars, Parallel, Powered, a class I device type, regulated under 21 CFR 890.5380. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
IRR
Device name
Bars, Parallel, Powered
Regulation
21 CFR 890.5380
Device class
Class I
Review panel
Physical Medicine
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 IRR

By decision year
1 clearance under product code IRR with a decision year between 1994 and 1994, 1994 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IRR by decision year
YearClearances
19941

Applicants with the most clearances

Product code IRR
Applicants holding the most 510(k) clearances under product code IRR
ApplicantClearances
Bailey Mfg. Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code