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FDA 510(k)

DATASCOPE MULTINEX II

K-Number: K926451 · 1993-08-25

ApplicantDatascope Corp.
Decision Date1993-08-25
Product CodeCBQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DATASCOPE MULTINEX II is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1993-08-25 under 510(k) number K926451. The device is classified under product code CBQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATASCOPE MULTINEX II?

DATASCOPE MULTINEX II is a medical device that received FDA 510(k) clearance on 1993-08-25. The listed applicant is Datascope Corp.. The 510(k) number is K926451.

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

DATASCOPE MULTINEX II received FDA 510(k) clearance on 1993-08-25, under 510(k) number K926451.

Who is the listed applicant for DATASCOPE MULTINEX II?

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 II?

The FDA product code for DATASCOPE MULTINEX II is CBQ.

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Related Devices (Code: CBQ)

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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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