AUTOMATED PHYSIOLOGIC PROFILE MONITOR— 510(k) K811560

Name: FDA 510(k) clearance K811560
Creator: U.S. Food and Drug Administration
Published: 1981-06-18

Substantially Equivalent

Life Sciences Manufacturing, Inc.

FDA 510(k) clearance K811560 for AUTOMATED PHYSIOLOGIC PROFILE MONITOR, Substantially Equivalent on 1981-06-18. Applicant: Life Sciences Manufacturing, Inc.. Device class: 2.

Clearance details

Applicant: Life Sciences Manufacturing, Inc.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1981-06-02
Decision date: 1981-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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