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
K872094Substantially Equivalent

Vacu-Aide

The Devilbiss Co., Somerset PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872094 is the FDA 510(k) clearance record for VACU-AIDE, a class II device, cleared for The Devilbiss Co. on under FDA product code JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered). FDA records list 12 510(k) clearances for The Devilbiss Co., from to . As of , FDA records show no recalls naming K872094.

Clearance record

Decision date
Received
(136 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
The Devilbiss Co. P.O. Box 635, Somerset PA
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