MODIFIED ASSESS(R) PEAK FLOW METER— 510(k) K896953

Name: FDA 510(k) clearance K896953
Creator: U.S. Food and Drug Administration
Published: 1990-01-30

Substantially Equivalent

Health Products, Inc.

FDA 510(k) clearance K896953 for MODIFIED ASSESS(R) PEAK FLOW METER, Substantially Equivalent on 1990-01-30. Applicant: Health Products, Inc.. Device class: 2.

Clearance details

Applicant: Health Products, Inc.
Product code: Code BZH
Device class: Class 2
Regulation: 21 CFR 868.1860
Advisory panel: Anesthesiology
Date received: 1989-12-05
Decision date: 1990-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cedar Grove, NJ, US

Download summary PDF View on FDA.gov ↗

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