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FDA 510(k)

KEGELMASTER 2000

K-Number: K023305 · 2002-12-26

ApplicantKegelmaster 2000 , Ltd.
Decision Date2002-12-26
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KEGELMASTER 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Kegelmaster 2000 , Ltd.. It received FDA 510(k) clearance on 2002-12-26 under 510(k) number K023305. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEGELMASTER 2000?

KEGELMASTER 2000 is a medical device that received FDA 510(k) clearance on 2002-12-26. The listed applicant is Kegelmaster 2000 , Ltd.. The 510(k) number is K023305.

When did KEGELMASTER 2000 receive FDA 510(k) clearance?

KEGELMASTER 2000 received FDA 510(k) clearance on 2002-12-26, under 510(k) number K023305.

Who is the listed applicant for KEGELMASTER 2000?

The FDA 510(k) record lists Kegelmaster 2000 , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KEGELMASTER 2000?

The FDA product code for KEGELMASTER 2000 is HIR.

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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.

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