EXERCISOR, RESPIRATORY— 510(k) K770619

Name: FDA 510(k) clearance K770619
Creator: U.S. Food and Drug Administration
Published: 1977-04-07

Substantially Equivalent

Cutter Laboratories, Inc.

FDA 510(k) clearance K770619 for EXERCISOR, RESPIRATORY, Substantially Equivalent on 1977-04-07. Applicant: Cutter Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Cutter Laboratories, Inc.
Product code: Code BWF
Device class: Class 2
Regulation: 21 CFR 868.5690
Advisory panel: Anesthesiology
Date received: 1977-04-01
Decision date: 1977-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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