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

Instrument, Dowel Cutting

21 CFR 882.4275 / Neurology
FDA source (opens on fda.gov)

GZQ is the FDA product code for Instrument, Dowel Cutting, a class II device type, regulated under 21 CFR 882.4275. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
GZQ
Device name
Instrument, Dowel Cutting
Regulation
21 CFR 882.4275
Device class
Class II
Review panel
Neurology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code GZQ

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

Applicants with the most clearances

Product code GZQ
Applicants holding the most 510(k) clearances under product code GZQ
ApplicantClearances
Altoona Medical Supply1

Companies listing this code with FDA

Companies whose registered establishments list this code