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FDA 510(k)

KAPLAN PENDULASER 115 - A 15W CO2 SURGICAL LASER

K-Number: K950313 · 1995-03-24

Decision Date1995-03-24
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KAPLAN PENDULASER 115 - A 15W CO2 SURGICAL LASER is the device name listed in this FDA 510(k) record. The listed applicant is Optomedic Medical Technologies , Ltd.. It received FDA 510(k) clearance on 1995-03-24 under 510(k) number K950313. 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 KAPLAN PENDULASER 115 - A 15W CO2 SURGICAL LASER?

KAPLAN PENDULASER 115 - A 15W CO2 SURGICAL LASER is a medical device that received FDA 510(k) clearance on 1995-03-24. The listed applicant is Optomedic Medical Technologies , Ltd.. The 510(k) number is K950313.

When did KAPLAN PENDULASER 115 - A 15W CO2 SURGICAL LASER receive FDA 510(k) clearance?

KAPLAN PENDULASER 115 - A 15W CO2 SURGICAL LASER received FDA 510(k) clearance on 1995-03-24, under 510(k) number K950313.

Who is the listed applicant for KAPLAN PENDULASER 115 - A 15W CO2 SURGICAL LASER?

The FDA 510(k) record lists Optomedic Medical Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KAPLAN PENDULASER 115 - A 15W CO2 SURGICAL LASER?

The FDA product code for KAPLAN PENDULASER 115 - A 15W CO2 SURGICAL LASER is GEX. This falls under the Gastroenterology category.

Related Clinical Trials

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.

Other records listing Optomedic Medical Technologies , Ltd. 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.

Related Devices (Code: GEX)

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.

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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