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FDA 510(k)

DAN KERRISON RONGEURS, MODELS K1 + BILLY 1

K-Number: K023868 · 2003-02-07

ApplicantDannoritzer Medical Instruments
Decision Date2003-02-07
Product CodeHAE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DAN KERRISON RONGEURS, MODELS K1 + BILLY 1 is the device name listed in this FDA 510(k) record. The listed applicant is Dannoritzer Medical Instruments. It received FDA 510(k) clearance on 2003-02-07 under 510(k) number K023868. The device is classified under product code HAE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAN KERRISON RONGEURS, MODELS K1 + BILLY 1?

DAN KERRISON RONGEURS, MODELS K1 + BILLY 1 is a medical device that received FDA 510(k) clearance on 2003-02-07. The listed applicant is Dannoritzer Medical Instruments. The 510(k) number is K023868.

When did DAN KERRISON RONGEURS, MODELS K1 + BILLY 1 receive FDA 510(k) clearance?

DAN KERRISON RONGEURS, MODELS K1 + BILLY 1 received FDA 510(k) clearance on 2003-02-07, under 510(k) number K023868.

Who is the listed applicant for DAN KERRISON RONGEURS, MODELS K1 + BILLY 1?

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

What is the FDA product code for DAN KERRISON RONGEURS, MODELS K1 + BILLY 1?

The FDA product code for DAN KERRISON RONGEURS, MODELS K1 + BILLY 1 is HAE.

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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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