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FDA 510(k)

PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV

K-Number: K890182 · 1990-02-28

ApplicantAesculap Instruments Corp.
Decision Date1990-02-28
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap Instruments Corp.. It received FDA 510(k) clearance on 1990-02-28 under 510(k) number K890182. The device is classified under product code DSY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV?

PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV is a medical device that received FDA 510(k) clearance on 1990-02-28. The listed applicant is Aesculap Instruments Corp.. The 510(k) number is K890182.

When did PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV receive FDA 510(k) clearance?

PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV received FDA 510(k) clearance on 1990-02-28, under 510(k) number K890182.

Who is the listed applicant for PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV?

The FDA 510(k) record lists Aesculap Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV?

The FDA product code for PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV is DSY.

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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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