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FDA 510(k)

SHARPLAN 2100,3000,SHARPLASER 65, 40

K-Number: K920865 · 1993-08-02

ApplicantSharplan Lasers, Inc.
Decision Date1993-08-02
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHARPLAN 2100,3000,SHARPLASER 65, 40 is the device name listed in this FDA 510(k) record. The listed applicant is Sharplan Lasers, Inc.. It received FDA 510(k) clearance on 1993-08-02 under 510(k) number K920865. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARPLAN 2100,3000,SHARPLASER 65, 40?

SHARPLAN 2100,3000,SHARPLASER 65, 40 is a medical device that received FDA 510(k) clearance on 1993-08-02. The listed applicant is Sharplan Lasers, Inc.. The 510(k) number is K920865.

When did SHARPLAN 2100,3000,SHARPLASER 65, 40 receive FDA 510(k) clearance?

SHARPLAN 2100,3000,SHARPLASER 65, 40 received FDA 510(k) clearance on 1993-08-02, under 510(k) number K920865.

Who is the listed applicant for SHARPLAN 2100,3000,SHARPLASER 65, 40?

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

What is the FDA product code for SHARPLAN 2100,3000,SHARPLASER 65, 40?

The FDA product code for SHARPLAN 2100,3000,SHARPLASER 65, 40 is GEX. This falls under the Gastroenterology category.

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Other records listing Sharplan Lasers, Inc. as applicant

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Related Devices (Code: GEX)

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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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