510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K862154Substantially Equivalent

Venesection Equipment Storage Tray

Rmp Co., Fayetteville NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862154 is the FDA 510(k) clearance record for VENESECTION EQUIPMENT STORAGE TRAY, a class I device, cleared for Rmp Co. on under FDA product code FSM (Tray, Surgical, Instrument). FDA records list 2 510(k) clearances for Rmp Co., from to . As of , FDA records show no recalls naming K862154.

Clearance record

Decision date
Received
(11 days to decision)
Product code
FSM Tray, Surgical, Instrument
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Rmp Co. 6831 Uppingham Rd., Fayetteville NC
Third party review
No

Clearances, product code FSM

Trailing 12 months

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

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