510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K011229Substantially Equivalent

Devilbiss 9000 Series CPAP, Model 9001

Sunrise Medical Hhg, Inc., Somerset PA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K011229 is the FDA 510(k) clearance record for DEVILBISS 9000 SERIES CPAP, MODEL 9001, a class II device, cleared for Sunrise Medical Hhg, Inc. on under FDA product code BZD (Ventilator, Non-Continuous (Respirator)). FDA records list 10 510(k) clearances for Sunrise Medical Hhg, Inc., from to . As of , FDA records show no recalls naming K011229.

Clearance record

Decision date
Received
(79 days to decision)
Product code
BZD Ventilator, Non-Continuous (Respirator)
Regulation
21 CFR 868.5905
Device class
Class II
Review panel
Anesthesiology
Applicant
Sunrise Medical Hhg, Inc. 100 Devilbiss Dr., Somerset PA
510(k) summary
Summary
Third party review
No

Clearances, product code BZD

Trailing 12 months
11 clearances under product code BZD in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code BZD, trailing twelve months
MonthClearances
November 20250
December 20252
January 20262
February 20260
March 20260
April 20262
May 20262
June 20261
July 20261
August 20260
September 20261
October 20260