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FDA 510(k)

DATASCOPE/AVCO CONNECTOR

K-Number: K801601 · 1981-01-13

ApplicantDatascope Corp.
Decision Date1981-01-13
Product CodeDSP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DATASCOPE/AVCO CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1981-01-13 under 510(k) number K801601. The device is classified under product code DSP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATASCOPE/AVCO CONNECTOR?

DATASCOPE/AVCO CONNECTOR is a medical device that received FDA 510(k) clearance on 1981-01-13. The listed applicant is Datascope Corp.. The 510(k) number is K801601.

When did DATASCOPE/AVCO CONNECTOR receive FDA 510(k) clearance?

DATASCOPE/AVCO CONNECTOR received FDA 510(k) clearance on 1981-01-13, under 510(k) number K801601.

Who is the listed applicant for DATASCOPE/AVCO CONNECTOR?

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/AVCO CONNECTOR?

The FDA product code for DATASCOPE/AVCO CONNECTOR is DSP.

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Related Devices (Code: DSP)

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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