BRENTWOOD IQMARK DIGITAL SPIROMETER (INCLUDES DISPOSABLE PNEUMOTACH MOUTHPIECES AND 3-LITER CALIBRATION SYRINGE


the company

Device Classification Name

spirometer, diagnostic

510(k) Number K002499
Device Name BRENTWOOD IQMARK DIGITAL SPIROMETER (INCLUDES DISPOSABLE PNEUMOTACH MOUTHPIECES AND 3-LITER CALIBRATION SYRINGE
Original Applicant
BRENTWOOD MEDICAL TECHNOLOGY CORP.
3300 fujita st.
torrance, 
CA 
90505

Original Contact glen mizelle
Regulation Number 868.1840
Classification Product Code
BZG  
Date Received 08/14/2000
Decision Date 11/08/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Anesthesiology

510k Review Panel

Anesthesiology

Type Traditional
Reviewed by Third Party No

Combination Product

No