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

Curtain, Protective, Radiographic

21 CFR 892.6500 / Radiology
FDA source (opens on fda.gov)

IWQ is the FDA product code for Curtain, Protective, Radiographic, a class I device type, regulated under 21 CFR 892.6500. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IWQ
Device name
Curtain, Protective, Radiographic
Regulation
21 CFR 892.6500
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 IWQ

By decision year
3 clearances under product code IWQ with a decision year between 1989 and 1994, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IWQ by decision year
YearClearances
19891
19921
19941

Applicants with the most clearances

Product code IWQ
Applicants holding the most 510(k) clearances under product code IWQ
ApplicantClearances
F. Walter Hanel GmbH1
Hydro-Med Products, Inc.1
Techton, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 19 companies shown, in name order