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
K031413Substantially Equivalent

Vigormist Compressor Nebulizer

Vega Technologies Inc., Taipei, TW / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K031413 is the FDA 510(k) clearance record for VIGORMIST COMPRESSOR NEBULIZER, a class II device, cleared for Vega Technologies, Inc. on under FDA product code BTI (Compressor, Air, Portable). FDA records list 6 510(k) clearances for Vega Technologies, Inc., from to . As of , FDA records show one recall naming K031413.

Clearance record

Decision date
Received
(155 days to decision)
Product code
BTI Compressor, Air, Portable
Regulation
21 CFR 868.6250
Device class
Class II
Review panel
Anesthesiology
Applicant
Vega Technologies, Inc. 11f-13, 100 Chang-Chun Rd., Taipei, TW
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code BTI

Trailing 12 months

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

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