510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K040239Substantially Equivalent

Supraflow Console

Neomedix Corp., San Juan Capistrano CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K040239 is the FDA 510(k) clearance record for SUPRAFLOW CONSOLE, a class II device, cleared for Neomedix Corp. on under FDA product code BTA (Pump, Portable, Aspiration (Manual Or Powered)). FDA records list 4 510(k) clearances for Neomedix Corp., from to . As of , FDA records show one recall naming K040239.

Clearance record

Decision date
Received
(15 days to decision)
Product code
BTA Pump, Portable, Aspiration (Manual Or Powered)
Regulation
21 CFR 878.4780
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Neomedix Corp. 27452 Calle Arroyo, San Juan Capistrano CA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code BTA

Trailing 12 months
6 clearances under product code BTA in the twelve months to October 2026, May 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code BTA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20261
May 20264
June 20260
July 20260
August 20260
September 20260
October 20260