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

Processor, Cine Film

21 CFR 892.1900 / Radiology
FDA source (opens on fda.gov)

IXX is the FDA product code for Processor, Cine Film, a class II device type, regulated under 21 CFR 892.1900. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IXX
Device name
Processor, Cine Film
Regulation
21 CFR 892.1900
Device class
Class II
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
6
Ingested recalls
0

Clearances, product code IXX

By decision year
6 clearances under product code IXX with a decision year between 1984 and 1996, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IXX by decision year
YearClearances
19841
19851
19861
19911
19921
19961

Applicants with the most clearances

Product code IXX
Applicants holding the most 510(k) clearances under product code IXX
ApplicantClearances
The Allen Products Co.3
Jamieson Film Co.2
Anago, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code