SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR— 510(k) K863042

Name: FDA 510(k) clearance K863042
Creator: U.S. Food and Drug Administration
Published: 1987-01-14

Substantially Equivalent

Siemens Medical Solutions USA, Inc.

FDA 510(k) clearance K863042 for SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR, Substantially Equivalent on 1987-01-14. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 2.

Clearance details

Applicant: Siemens Medical Solutions USA, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1986-08-12
Decision date: 1987-01-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Iselin, NJ, US

Download summary PDF View on FDA.gov ↗

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