510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K803174Substantially Equivalent

Conphar Percussion Hammer(buck Type)

Conphar, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K803174 is the FDA 510(k) clearance record for CONPHAR PERCUSSION HAMMER(BUCK TYPE), a class I device, cleared for Conphar, Inc. on under FDA product code GWZ (Percussor). FDA records list 122 510(k) clearances for Conphar, Inc., from to . As of , FDA records show no recalls naming K803174.

Clearance record

Decision date
Received
(15 days to decision)
Product code
GWZ Percussor
Regulation
21 CFR 882.1700
Device class
Class I
Review panel
Neurology
Applicant
Conphar, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GWZ

Trailing 12 months

FDA records hold no clearances under product code GWZ in the trailing twelve months.

FDA records show no clearances under product code GWZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GWZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260