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FDA 510(k)

PERCOR PERCUTANEOUS INTRODUCER

K-Number: K820834 · 1982-04-14

ApplicantDatascope Corp.
Decision Date1982-04-14
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERCOR PERCUTANEOUS INTRODUCER is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1982-04-14 under 510(k) number K820834. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCOR PERCUTANEOUS INTRODUCER?

PERCOR PERCUTANEOUS INTRODUCER is a medical device that received FDA 510(k) clearance on 1982-04-14. The listed applicant is Datascope Corp.. The 510(k) number is K820834.

When did PERCOR PERCUTANEOUS INTRODUCER receive FDA 510(k) clearance?

PERCOR PERCUTANEOUS INTRODUCER received FDA 510(k) clearance on 1982-04-14, under 510(k) number K820834.

Who is the listed applicant for PERCOR PERCUTANEOUS INTRODUCER?

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 PERCOR PERCUTANEOUS INTRODUCER?

The FDA product code for PERCOR PERCUTANEOUS INTRODUCER is DYB.

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Related Devices (Code: DYB)

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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