BLOOD PRESSURE, DIGITAL MODEL #2153— 510(k) K781701

Name: FDA 510(k) clearance K781701
Creator: U.S. Food and Drug Administration
Published: 1978-12-04

Substantially Equivalent

Sears, Roebuck & Co.

FDA 510(k) clearance K781701 for BLOOD PRESSURE, DIGITAL MODEL #2153, Substantially Equivalent on 1978-12-04. 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: 1978-10-10
Decision date: 1978-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K810635 — ELECTRODE BLOOD PRESSURE MONITOR1981-05-08
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K780986 — DIGITAL BLOOD PRESSURE MONITOR1978-07-18
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