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

Percussor

21 CFR 882.1700 / Neurology
FDA source (opens on fda.gov)

GWZ is the FDA product code for Percussor, a class I device type, regulated under 21 CFR 882.1700. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GWZ
Device name
Percussor
Regulation
21 CFR 882.1700
Device class
Class I
Review panel
Neurology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
11
Ingested recalls
0

Clearances, product code GWZ

By decision year
11 clearances under product code GWZ with a decision year between 1979 and 1989, 1984 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code GWZ by decision year
YearClearances
19792
19801
19812
19843
19852
19891

Applicants with the most clearances

Product code GWZ
Applicants holding the most 510(k) clearances under product code GWZ
ApplicantClearances
Imm Enterprises, Ltd.3
Amdia Medical Products2
Conphar, Inc.2
Artiberia1
Robert I. Chien & Assoc., Inc.1
Sandal Surgico1
The Huxley Instrument Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 63 companies shown, in name order