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

Phantom, Anthropomorphic, Nuclear

21 CFR 892.1370 / Radiology
FDA source (opens on fda.gov)

IYP is the FDA product code for Phantom, Anthropomorphic, Nuclear, a class I device type, regulated under 21 CFR 892.1370. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IYP
Device name
Phantom, Anthropomorphic, Nuclear
Regulation
21 CFR 892.1370
Device class
Class I
Review panel
Radiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code IYP

By decision year
3 clearances under product code IYP with a decision year between 1981 and 1992, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IYP by decision year
YearClearances
19811
19851
19921

Applicants with the most clearances

Product code IYP
Applicants holding the most 510(k) clearances under product code IYP
ApplicantClearances
Circadian, Inc.1
Elscint, Inc.1
Mick Radio-Nuclear Instruments, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code