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

Rotator, Transverse

21 CFR 890.3025 / Physical Medicine
FDA source (opens on fda.gov)

IQP is the FDA product code for Rotator, Transverse, a class I device type, regulated under 21 CFR 890.3025. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
IQP
Device name
Rotator, Transverse
Regulation
21 CFR 890.3025
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code IQP

By decision year
1 clearance under product code IQP with a decision year between 1979 and 1979, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IQP by decision year
YearClearances
19791

Applicants with the most clearances

Product code IQP
Applicants holding the most 510(k) clearances under product code IQP
ApplicantClearances
Parke-Davis Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code