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
K140929Substantially Equivalent

Z1 CPAP System

Breas Medical AB, North Reading MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K140929 is the FDA 510(k) clearance record for Z1 CPAP SYSTEM, a class II device, cleared for Human Design Medical, LLC on under FDA product code BZD (Ventilator, Non-Continuous (Respirator)). FDA records list 16 510(k) clearances for BREAS MEDICAL AB, from to . As of , FDA records show no recalls naming K140929.

Clearance record

Decision date
Received
(191 days to decision)
Product code
BZD Ventilator, Non-Continuous (Respirator)
Regulation
21 CFR 868.5905
Device class
Class II
Review panel
Anesthesiology
Applicant
Human Design Medical, LLC 5 Timber Ln., North Reading MA
510(k) summary
Summary PDF
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