510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K030838Substantially Equivalent

Wartner Pro

Wartner Medical Products, Richmond Hill, Ontario, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030838 is the FDA 510(k) clearance record for WARTNER PRO, a class II device, cleared for Wartner Medical Products on under FDA product code GEH (Unit, Cryosurgical, Accessories). FDA records list 3 510(k) clearances for Wartner Medical Products, from to . As of , FDA records show no recalls naming K030838.

Clearance record

Decision date
Received
(102 days to decision)
Product code
GEH Unit, Cryosurgical, Accessories
Regulation
21 CFR 878.4350
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Wartner Medical Products 65 Ava Crescent, Richmond Hill, Ontario, CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GEH

Trailing 12 months
9 clearances under product code GEH in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code GEH, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20262
March 20260
April 20262
May 20260
June 20262
July 20260
August 20260
September 20261
October 20260