LDW SPIROMETRY SYSTEM— 510(k) K896300

Name: FDA 510(k) clearance K896300
Creator: U.S. Food and Drug Administration
Published: 1990-04-03

Substantially Equivalent

Lanpher Diagnostic Workstations, Inc.

FDA 510(k) clearance K896300 for LDW SPIROMETRY SYSTEM, Substantially Equivalent on 1990-04-03. Applicant: Lanpher Diagnostic Workstations, Inc.. Device class: 2.

Clearance details

Applicant: Lanpher Diagnostic Workstations, Inc.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1989-10-30
Decision date: 1990-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Atherton, CA, US

Download summary PDF View on FDA.gov ↗

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