510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K900566Substantially Equivalent

Richard-Allan Vessel Loops

Richard-Allan Medical Ind., Inc., Richland MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900566 is the FDA 510(k) clearance record for RICHARD-ALLAN VESSEL LOOPS, a class I device, cleared for Richard-Allan Medical Ind., Inc. on under FDA product code KDC (Instrument, Surgical, Disposable). FDA records list 33 510(k) clearances for Richard-Allan Medical Ind., Inc., from to . As of , FDA records show no recalls naming K900566.

Clearance record

Decision date
Received
(85 days to decision)
Product code
KDC Instrument, Surgical, Disposable
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Richard-Allan Medical Ind., Inc. 8850m89, Box 351, Richland MI
Third party review
No

Clearances, product code KDC

Trailing 12 months

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

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