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FDA 510(k)

GRAFT TUNNELER

K-Number: K790124 · 1979-02-08

ApplicantNarco Scientific
Decision Date1979-02-08
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GRAFT TUNNELER is the device name listed in this FDA 510(k) record. The listed applicant is Narco Scientific. It received FDA 510(k) clearance on 1979-02-08 under 510(k) number K790124. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAFT TUNNELER?

GRAFT TUNNELER is a medical device that received FDA 510(k) clearance on 1979-02-08. The listed applicant is Narco Scientific. The 510(k) number is K790124.

When did GRAFT TUNNELER receive FDA 510(k) clearance?

GRAFT TUNNELER received FDA 510(k) clearance on 1979-02-08, under 510(k) number K790124.

Who is the listed applicant for GRAFT TUNNELER?

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

What is the FDA product code for GRAFT TUNNELER?

The FDA product code for GRAFT TUNNELER is DWS.

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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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