510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K791239Substantially Equivalent

Briox Model 2000-a Aspirator Unit

Briox Technologies, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K791239 is the FDA 510(k) clearance record for BRIOX MODEL 2000-A ASPIRATOR UNIT, a class II device, cleared for Briox Technologies, Inc. on under FDA product code JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered). FDA records list 6 510(k) clearances for Briox Technologies, Inc., from to . As of , FDA records show no recalls naming K791239.

Clearance record

Decision date
Received
(18 days to decision)
Product code
JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered
Regulation
21 CFR 878.4780
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Briox Technologies, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JCX

Trailing 12 months
1 clearance under product code JCX in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JCX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260