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FDA 510(k)

GYNE IDEAS MINITAPE RP DEVICE

K-Number: K023898 · 2003-06-18

ApplicantGyne Ideas , Ltd.
Decision Date2003-06-18
Product CodePAH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GYNE IDEAS MINITAPE RP DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Gyne Ideas , Ltd.. It received FDA 510(k) clearance on 2003-06-18 under 510(k) number K023898. The device is classified under product code PAH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GYNE IDEAS MINITAPE RP DEVICE?

GYNE IDEAS MINITAPE RP DEVICE is a medical device that received FDA 510(k) clearance on 2003-06-18. The listed applicant is Gyne Ideas , Ltd.. The 510(k) number is K023898.

When did GYNE IDEAS MINITAPE RP DEVICE receive FDA 510(k) clearance?

GYNE IDEAS MINITAPE RP DEVICE received FDA 510(k) clearance on 2003-06-18, under 510(k) number K023898.

Who is the listed applicant for GYNE IDEAS MINITAPE RP DEVICE?

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

What is the FDA product code for GYNE IDEAS MINITAPE RP DEVICE?

The FDA product code for GYNE IDEAS MINITAPE RP DEVICE is PAH.

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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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