510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K860571Substantially Equivalent

F.m. Weist,kg (Urodynamic Systems)

F.M. Wiest USA, Inc., Cherry Hill NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860571 is the FDA 510(k) clearance record for F.M. WEIST,KG (URODYNAMIC SYSTEMS), a class II device, cleared for F.M. Wiest USA, Inc. on under FDA product code FAP (Cystometric Gas (Carbon-Dioxide) On Hydraulic Device). FDA records list 12 510(k) clearances for F.M. Wiest USA, Inc., from to . As of , FDA records show no recalls naming K860571.

Clearance record

Decision date
Received
(32 days to decision)
Product code
FAP Cystometric Gas (Carbon-Dioxide) On Hydraulic Device
Regulation
21 CFR 876.1620
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
F.M. Wiest USA, Inc. 1301 N. Kings Hwy., Cherry Hill NJ
Third party review
No

Clearances, product code FAP

Trailing 12 months

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

FDA records show no clearances under product code FAP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FAP, 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