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FDA 510(k)

NIBP NON-INVAS. BLOOD PRESS. CART. MODEL 88 35 340

K-Number: K864737 · 1987-03-12

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1987-03-12
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NIBP NON-INVAS. BLOOD PRESS. CART. MODEL 88 35 340 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 1987-03-12 under 510(k) number K864737. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIBP NON-INVAS. BLOOD PRESS. CART. MODEL 88 35 340?

NIBP NON-INVAS. BLOOD PRESS. CART. MODEL 88 35 340 is a medical device that received FDA 510(k) clearance on 1987-03-12. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K864737.

When did NIBP NON-INVAS. BLOOD PRESS. CART. MODEL 88 35 340 receive FDA 510(k) clearance?

NIBP NON-INVAS. BLOOD PRESS. CART. MODEL 88 35 340 received FDA 510(k) clearance on 1987-03-12, under 510(k) number K864737.

Who is the listed applicant for NIBP NON-INVAS. BLOOD PRESS. CART. MODEL 88 35 340?

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 NIBP NON-INVAS. BLOOD PRESS. CART. MODEL 88 35 340?

The FDA product code for NIBP NON-INVAS. BLOOD PRESS. CART. MODEL 88 35 340 is DXN.

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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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