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

Adaptor, Holder, Syringe

21 CFR 890.5050 / Physical Medicine
FDA source (opens on fda.gov)

IQG is the FDA product code for Adaptor, Holder, Syringe, a class I device type, regulated under 21 CFR 890.5050. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IQG
Device name
Adaptor, Holder, Syringe
Regulation
21 CFR 890.5050
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
3
Ingested recalls
0

Clearances, product code IQG

By decision year
3 clearances under product code IQG with a decision year between 2006 and 2008, 2008 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code IQG by decision year
YearClearances
20061
20082

Applicants with the most clearances

Product code IQG
Applicants holding the most 510(k) clearances under product code IQG
ApplicantClearances
41 Industries, LLC1
Abbott Medical1
Medicool, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 77 companies shown, in name order