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FDA 510(k)

EIDOLON ENDOSCOPE COUPLER

K-Number: K942141 · 1994-05-27

ApplicantEidolon Corp.
Decision Date1994-05-27
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EIDOLON ENDOSCOPE COUPLER is the device name listed in this FDA 510(k) record. The listed applicant is Eidolon Corp.. It received FDA 510(k) clearance on 1994-05-27 under 510(k) number K942141. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EIDOLON ENDOSCOPE COUPLER?

EIDOLON ENDOSCOPE COUPLER is a medical device that received FDA 510(k) clearance on 1994-05-27. The listed applicant is Eidolon Corp.. The 510(k) number is K942141.

When did EIDOLON ENDOSCOPE COUPLER receive FDA 510(k) clearance?

EIDOLON ENDOSCOPE COUPLER received FDA 510(k) clearance on 1994-05-27, under 510(k) number K942141.

Who is the listed applicant for EIDOLON ENDOSCOPE COUPLER?

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

What is the FDA product code for EIDOLON ENDOSCOPE COUPLER?

The FDA product code for EIDOLON ENDOSCOPE COUPLER is FET.

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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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