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FDA 510(k)

SHARPLAN MEDILAS 4060 N

K-Number: K882037 · 1988-06-20

ApplicantSharplan Lasers, Inc.
Decision Date1988-06-20
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHARPLAN MEDILAS 4060 N 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 1988-06-20 under 510(k) number K882037. 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 MEDILAS 4060 N?

SHARPLAN MEDILAS 4060 N is a medical device that received FDA 510(k) clearance on 1988-06-20. The listed applicant is Sharplan Lasers, Inc.. The 510(k) number is K882037.

When did SHARPLAN MEDILAS 4060 N receive FDA 510(k) clearance?

SHARPLAN MEDILAS 4060 N received FDA 510(k) clearance on 1988-06-20, under 510(k) number K882037.

Who is the listed applicant for SHARPLAN MEDILAS 4060 N?

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 MEDILAS 4060 N?

The FDA product code for SHARPLAN MEDILAS 4060 N is GEX. This falls under the Gastroenterology category.

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Other records listing Sharplan Lasers, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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