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FDA 510(k)

DATASCOPE MULTINEX ID MONITOR

K-Number: K910106 · 1991-03-29

ApplicantDatascope Corp.
Decision Date1991-03-29
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DATASCOPE MULTINEX ID MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1991-03-29 under 510(k) number K910106. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATASCOPE MULTINEX ID MONITOR?

DATASCOPE MULTINEX ID MONITOR is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Datascope Corp.. The 510(k) number is K910106.

When did DATASCOPE MULTINEX ID MONITOR receive FDA 510(k) clearance?

DATASCOPE MULTINEX ID MONITOR received FDA 510(k) clearance on 1991-03-29, under 510(k) number K910106.

Who is the listed applicant for DATASCOPE MULTINEX ID MONITOR?

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 DATASCOPE MULTINEX ID MONITOR?

The FDA product code for DATASCOPE MULTINEX ID MONITOR is CCK.

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Related Devices (Code: CCK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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