Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS

K-Number: K880550 · 1988-07-25

ApplicantMedimicro Systems, Inc.
Decision Date1988-07-25
Product CodeBZM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS is the device name listed in this FDA 510(k) record. The listed applicant is Medimicro Systems, Inc.. It received FDA 510(k) clearance on 1988-07-25 under 510(k) number K880550. The device is classified under product code BZM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS?

BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS is a medical device that received FDA 510(k) clearance on 1988-07-25. The listed applicant is Medimicro Systems, Inc.. The 510(k) number is K880550.

When did BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS receive FDA 510(k) clearance?

BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS received FDA 510(k) clearance on 1988-07-25, under 510(k) number K880550.

Who is the listed applicant for BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS?

The FDA 510(k) record lists Medimicro Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS?

The FDA product code for BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS is BZM.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: BZM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K102229PULMOTRACK 2020 SYSTEMKarmelsonixK090863PERSONAL WHEEZOMETERKarmelsonixK071955WIM-PC, MODEL 1010KarmelsonixK012387STG MULTICHANNEL LUNG SOUND ANALYSIS SYSTEMStethographics, Inc.K980878PULMOTRACK,MODEL 1010Karmel Medical Acoustic Technologies , Ltd.K974200ORCA CARDIOPULMONARY EXERCISE TESTING SYSTEMOrca Diagnostics Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑