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FDA 510(k)

MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKE

K-Number: K913104 · 1991-07-31

ApplicantDexide, Inc.
Decision Date1991-07-31
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKE is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1991-07-31 under 510(k) number K913104. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKE?

MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKE is a medical device that received FDA 510(k) clearance on 1991-07-31. The listed applicant is Dexide, Inc.. The 510(k) number is K913104.

When did MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKE receive FDA 510(k) clearance?

MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKE received FDA 510(k) clearance on 1991-07-31, under 510(k) number K913104.

Who is the listed applicant for MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKE?

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

What is the FDA product code for MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKE?

The FDA product code for MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKE is GCJ.

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Other records listing Dexide, Inc. as applicant

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Related Devices (Code: GCJ)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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