AMP PORTABLE PATIENT PRESSURE MONITOR— 510(k) K802600

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..

Clearance details

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

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