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

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..

Clearance details

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

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