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FDA 510(k)

VIEWPOINT CENTRAL MONITORING SYSTEM, MODEL 0998-00-0187-07

K-Number: K011540 · 2002-02-06

ApplicantDatascope Corp.
Decision Date2002-02-06
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VIEWPOINT CENTRAL MONITORING SYSTEM, MODEL 0998-00-0187-07 is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 2002-02-06 under 510(k) number K011540. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIEWPOINT CENTRAL MONITORING SYSTEM, MODEL 0998-00-0187-07?

VIEWPOINT CENTRAL MONITORING SYSTEM, MODEL 0998-00-0187-07 is a medical device that received FDA 510(k) clearance on 2002-02-06. The listed applicant is Datascope Corp.. The 510(k) number is K011540.

When did VIEWPOINT CENTRAL MONITORING SYSTEM, MODEL 0998-00-0187-07 receive FDA 510(k) clearance?

VIEWPOINT CENTRAL MONITORING SYSTEM, MODEL 0998-00-0187-07 received FDA 510(k) clearance on 2002-02-06, under 510(k) number K011540.

Who is the listed applicant for VIEWPOINT CENTRAL MONITORING SYSTEM, MODEL 0998-00-0187-07?

The FDA 510(k) record lists Datascope Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIEWPOINT CENTRAL MONITORING SYSTEM, MODEL 0998-00-0187-07?

The FDA product code for VIEWPOINT CENTRAL MONITORING SYSTEM, MODEL 0998-00-0187-07 is MHX.

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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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