510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K913487Substantially Equivalent

Riwolith 2280

Richard Wolf Medical Instruments Corp., Rosemont IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913487 is the FDA 510(k) clearance record for RIWOLITH 2280, a class II device, cleared for Richard Wolf Medical Instruments Corp. on under FDA product code FFK (Lithotriptor, Electro-Hydraulic). FDA records list 153 510(k) clearances for Richard Wolf Medical Instruments Corp., from to . As of , FDA records show no recalls naming K913487.

Clearance record

Decision date
Received
(183 days to decision)
Product code
FFK Lithotriptor, Electro-Hydraulic
Regulation
21 CFR 876.4480
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Richard Wolf Medical Instruments Corp. 7046 Lyndon Ave., Rosemont IL
510(k) summary
Statement
Third party review
No

Clearances, product code FFK

Trailing 12 months

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

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