510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K210077Substantially Equivalent

Med RF 4000

F Care Systems USA, Miami FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K210077 is the FDA 510(k) clearance record for MED RF 4000, a class II device, cleared for F Care Systems USA, LLC on under FDA product code ONQ (Electrosurgical Coagulation For Aesthetic). FDA's definition for product code ONQ reads: "For the treatment of spider vein or telangiectasia by thermocoagulation". FDA records list 4 510(k) clearances for F Care Systems USA, LLC, from to . As of , FDA records show no recalls naming K210077.

Clearance record

Decision date
Received
(339 days to decision)
Product code
ONQ Electrosurgical Coagulation For Aesthetic
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
F Care Systems USA, LLC 11098 Biscayne Blvd. Suite 301, Miami FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ONQ

Trailing 12 months

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

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