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FDA 510(k)

EPILIGHT HAIR REMOVAL SYSTEM

K-Number: K963249 · 1997-07-07

ApplicantEsc Medical Systems , Ltd.
Decision Date1997-07-07
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EPILIGHT HAIR REMOVAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Esc Medical Systems , Ltd.. It received FDA 510(k) clearance on 1997-07-07 under 510(k) number K963249. 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 EPILIGHT HAIR REMOVAL SYSTEM?

EPILIGHT HAIR REMOVAL SYSTEM is a medical device that received FDA 510(k) clearance on 1997-07-07. The listed applicant is Esc Medical Systems , Ltd.. The 510(k) number is K963249.

When did EPILIGHT HAIR REMOVAL SYSTEM receive FDA 510(k) clearance?

EPILIGHT HAIR REMOVAL SYSTEM received FDA 510(k) clearance on 1997-07-07, under 510(k) number K963249.

Who is the listed applicant for EPILIGHT HAIR REMOVAL SYSTEM?

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

What is the FDA product code for EPILIGHT HAIR REMOVAL SYSTEM?

The FDA product code for EPILIGHT HAIR REMOVAL SYSTEM is GEX. This falls under the Gastroenterology category.

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Other records listing Esc Medical Systems , 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.

K994014ESC INTENSE PULSED LIGHT SYSTEMS: EPILIGHT AND MULTILIGHTK991935EPILIGHT HAIR REMOVAL SYSTEM, PHOTODERM HR SYSTEMK982119DIODE LASERK974536PHOTODERM HR SYSTEMK980537ND: YAG ACCESSORY FOR PHOTODERM SYSTEMK972872DERMA K LASER SYSTEM

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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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