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FDA 510(k)

SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR

K-Number: K863042 · 1987-01-14

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1987-01-14
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1987-01-14 under 510(k) number K863042. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR?

SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR is a medical device that received FDA 510(k) clearance on 1987-01-14. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K863042.

When did SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR receive FDA 510(k) clearance?

SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR received FDA 510(k) clearance on 1987-01-14, under 510(k) number K863042.

Who is the listed applicant for SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR?

The FDA product code for SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR is DSK.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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