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

Transilluminator, Fiber Optic

21 CFR 874.4350 / Ear, Nose, Throat
FDA source (opens on fda.gov)

MQW is the FDA product code for Transilluminator, Fiber Optic, a class I device type, regulated under 21 CFR 874.4350. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
MQW
Device name
Transilluminator, Fiber Optic
Regulation
21 CFR 874.4350
Device class
Class I
Review panel
Ear, Nose, Throat
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 MQW

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

Applicants with the most clearances

Product code MQW
Applicants holding the most 510(k) clearances under product code MQW
ApplicantClearances
Karl Storz Endoscopy-America, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code