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FDA 510(k)

O'REGAN DISPOSABLE ANOSCOPE

K-Number: K020702 · 2002-03-29

ApplicantCanadian Theatre Products , Ltd.
Decision Date2002-03-29
Product CodeFER
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

O'REGAN DISPOSABLE ANOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Canadian Theatre Products , Ltd.. It received FDA 510(k) clearance on 2002-03-29 under 510(k) number K020702. The device is classified under product code FER. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the O'REGAN DISPOSABLE ANOSCOPE?

O'REGAN DISPOSABLE ANOSCOPE is a medical device that received FDA 510(k) clearance on 2002-03-29. The listed applicant is Canadian Theatre Products , Ltd.. The 510(k) number is K020702.

When did O'REGAN DISPOSABLE ANOSCOPE receive FDA 510(k) clearance?

O'REGAN DISPOSABLE ANOSCOPE received FDA 510(k) clearance on 2002-03-29, under 510(k) number K020702.

Who is the listed applicant for O'REGAN DISPOSABLE ANOSCOPE?

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

What is the FDA product code for O'REGAN DISPOSABLE ANOSCOPE?

The FDA product code for O'REGAN DISPOSABLE ANOSCOPE is FER.

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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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