AMP PORTABLE PATIENT PRESSURE MONITOR— 510(k) K802600

Name: FDA 510(k) clearance K802600
Creator: U.S. Food and Drug Administration
Published: 1980-11-12

Substantially Equivalent

American Medical Products, Inc.

FDA 510(k) clearance K802600 for AMP PORTABLE PATIENT PRESSURE MONITOR, Substantially Equivalent on 1980-11-12. Applicant: American Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: American Medical Products, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1980-10-21
Decision date: 1980-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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