MICROLIFE AUTOMATIC BLOOD PRESSURE MONITOR— 510(k) K970211

Name: FDA 510(k) clearance K970211
Creator: U.S. Food and Drug Administration
Published: 1998-04-30

Substantially Equivalent

Micro Weiss Electronics

FDA 510(k) clearance K970211 for MICROLIFE AUTOMATIC BLOOD PRESSURE MONITOR, Substantially Equivalent on 1998-04-30. Applicant: Micro Weiss Electronics. Device class: 2.

Clearance details

Applicant: Micro Weiss Electronics
Product code: Code DPW
Device class: Class 2
Regulation: 21 CFR 870.2100
Advisory panel: Cardiovascular
Date received: 1997-01-21
Decision date: 1998-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck,, NY, US

Download summary PDF View on FDA.gov ↗

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