FDA 510(k)

DATASCOPE PERCOR PERCUTANEOUS INTRODUCER W/PEELABL

K-Number: K902932 · 1990-10-16

Decision Date1990-10-16

Product CodeDYB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

DATASCOPE PERCOR PERCUTANEOUS INTRODUCER W/PEELABL is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1990-10-16 under 510(k) number K902932. 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 DATASCOPE PERCOR PERCUTANEOUS INTRODUCER W/PEELABL?

DATASCOPE PERCOR PERCUTANEOUS INTRODUCER W/PEELABL is a medical device that received FDA 510(k) clearance on 1990-10-16. The listed applicant is Datascope Corp.. The 510(k) number is K902932.

When did DATASCOPE PERCOR PERCUTANEOUS INTRODUCER W/PEELABL receive FDA 510(k) clearance?

DATASCOPE PERCOR PERCUTANEOUS INTRODUCER W/PEELABL received FDA 510(k) clearance on 1990-10-16, under 510(k) number K902932.

Who is the listed applicant for DATASCOPE PERCOR PERCUTANEOUS INTRODUCER W/PEELABL?

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 PERCOR PERCUTANEOUS INTRODUCER W/PEELABL?

The FDA product code for DATASCOPE PERCOR PERCUTANEOUS INTRODUCER W/PEELABL is DYB.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.