LME BLOOD PRESSURE MONITOR— 510(k) K832017

Name: FDA 510(k) clearance K832017
Creator: U.S. Food and Drug Administration
Published: 1983-10-31

Substantially Equivalent

Litton Medical Electronics

FDA 510(k) clearance K832017 for LME BLOOD PRESSURE MONITOR, Substantially Equivalent on 1983-10-31. Applicant: Litton Medical Electronics. Device class: 2.

Clearance details

Applicant: Litton Medical Electronics
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1983-06-23
Decision date: 1983-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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