BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS— 510(k) K880550

Name: FDA 510(k) clearance K880550
Creator: U.S. Food and Drug Administration
Published: 1988-07-25

Substantially Equivalent

Medimicro Systems, Inc.

FDA 510(k) clearance K880550 for BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS, Substantially Equivalent on 1988-07-25. Applicant: Medimicro Systems, Inc.. Device class: 2.

Clearance details

Applicant: Medimicro Systems, Inc.
Product code: Code BZM
Device class: Class 2
Regulation: 21 CFR 868.1900
Advisory panel: Anesthesiology
Date received: 1988-02-09
Decision date: 1988-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucson, AZ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BZM

view all

K102229 — PULMOTRACK 2020 SYSTEM2011-03-04
K090863 — PERSONAL WHEEZOMETER2009-09-21
K071955 — WIM-PC, MODEL 10102007-11-01
K012387 — STG MULTICHANNEL LUNG SOUND ANALYSIS SYSTEM2002-04-23
K980878 — PULMOTRACK,MODEL 10101998-12-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.