ELECTRODE BLOOD PRESSURE MONITOR— 510(k) K810635

Name: FDA 510(k) clearance K810635
Creator: U.S. Food and Drug Administration
Published: 1981-05-08

Substantially Equivalent

Sears, Roebuck & Co.

FDA 510(k) clearance K810635 for ELECTRODE BLOOD PRESSURE MONITOR, Substantially Equivalent on 1981-05-08. Applicant: Sears, Roebuck & Co.. Device class: 2.

Clearance details

Applicant: Sears, Roebuck & Co.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1981-03-10
Decision date: 1981-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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