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
K002499Substantially Equivalent

Brentwood Iqmark Digital Spirometer (Includes Disposable Pneumotach Mouthpieces and 3-Liter Calibration Syringe

Brentwood Medical Technology Corp., Torrance CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002499 is the FDA 510(k) clearance record for BRENTWOOD IQMARK DIGITAL SPIROMETER (INCLUDES DISPOSABLE PNEUMOTACH MOUTHPIECES AND 3-LITER CALIBRATION SYRINGE, a class II device, cleared for Brentwood Medical Technology Corp. on under FDA product code BZG (Spirometer, Diagnostic). FDA records list 7 510(k) clearances for Brentwood Medical Technology Corp., from to . As of , FDA records show no recalls naming K002499.

Clearance record

Decision date
Received
(86 days to decision)
Product code
BZG Spirometer, Diagnostic
Regulation
21 CFR 868.1840
Device class
Class II
Review panel
Anesthesiology
Applicant
Brentwood Medical Technology Corp. 3300 Fujita St., Torrance CA
510(k) summary
Summary
Third party review
No

Clearances, product code BZG

Trailing 12 months
1 clearance under product code BZG in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code BZG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260