FDA 510(k)

SUCTION IRRIGATION CAUTERY PROBE

K-Number: K922002 · 1992-09-02

ApplicantMegadyne Medical Products, Inc.

Decision Date1992-09-02

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SUCTION IRRIGATION CAUTERY PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Megadyne Medical Products, Inc.. It received FDA 510(k) clearance on 1992-09-02 under 510(k) number K922002. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION IRRIGATION CAUTERY PROBE?

SUCTION IRRIGATION CAUTERY PROBE is a medical device that received FDA 510(k) clearance on 1992-09-02. The listed applicant is Megadyne Medical Products, Inc.. The 510(k) number is K922002.

When did SUCTION IRRIGATION CAUTERY PROBE receive FDA 510(k) clearance?

SUCTION IRRIGATION CAUTERY PROBE received FDA 510(k) clearance on 1992-09-02, under 510(k) number K922002.

Who is the listed applicant for SUCTION IRRIGATION CAUTERY PROBE?

The FDA 510(k) record lists Megadyne Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION IRRIGATION CAUTERY PROBE?

The FDA product code for SUCTION IRRIGATION CAUTERY PROBE is GEI.

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Other records listing Megadyne Medical Products, Inc. as applicant

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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.