510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K961126Substantially Equivalent

Pulse Dose Series

Devilbiss Health Care, Inc., Somerset PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K961126 is the FDA 510(k) clearance record for PULSE DOSE SERIES, a class II device, cleared for Devilbiss Health Care, Inc. on under FDA product code NFB (Conserver, Oxygen). FDA records list 29 510(k) clearances for Devilbiss Health Care, Inc., from to . As of , FDA records show no recalls naming K961126.

Clearance record

Decision date
Received
(214 days to decision)
Product code
NFB Conserver, Oxygen
Regulation
21 CFR 868.5905
Device class
Class II
Review panel
Anesthesiology
Applicant
Devilbiss Health Care, Inc. 1200 E. Main St., Somerset PA
510(k) summary
Summary
Third party review
No

Clearances, product code NFB

Trailing 12 months

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

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