510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K093617Substantially Equivalent

Ventlab 6000 Series Humidifier

Salter Labs, Mocksville NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K093617 is the FDA 510(k) clearance record for VENTLAB 6000 SERIES HUMIDIFIER, a class II device, cleared for Ventlab Corp. on under FDA product code BTT (Humidifier, Respiratory Gas, (Direct Patient Interface)). FDA records list 74 510(k) clearances for Salter Labs, from to . As of , FDA records show no recalls naming K093617.

Clearance record

Decision date
Received
(430 days to decision)
Product code
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
Regulation
21 CFR 868.5450
Device class
Class II
Review panel
Anesthesiology
Applicant
Ventlab Corp. 155 Boyce Dr., Mocksville NC
510(k) summary
Statement
Third party review
No

Clearances, product code BTT

Trailing 12 months
5 clearances under product code BTT in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code BTT, trailing twelve months
MonthClearances
November 20250
December 20251
January 20262
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260