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

Light Source, Incandescent, Diagnostic

21 CFR 876.1500 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FCQ is the FDA product code for Light Source, Incandescent, Diagnostic, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
FCQ
Device name
Light Source, Incandescent, Diagnostic
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code FCQ

By decision year
1 clearance under product code FCQ with a decision year between 1996 and 1996, 1996 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FCQ by decision year
YearClearances
19961

Applicants with the most clearances

Product code FCQ
Applicants holding the most 510(k) clearances under product code FCQ
ApplicantClearances
Mitsubishi Cable America, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code