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FDA 510(k)

PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS

K-Number: K022569 · 2002-08-29

ApplicantMedical Bio Care Sweden AB
Decision Date2002-08-29
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Bio Care Sweden AB. It received FDA 510(k) clearance on 2002-08-29 under 510(k) number K022569. 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 PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS?

PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS is a medical device that received FDA 510(k) clearance on 2002-08-29. The listed applicant is Medical Bio Care Sweden AB. The 510(k) number is K022569.

When did PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS receive FDA 510(k) clearance?

PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS received FDA 510(k) clearance on 2002-08-29, under 510(k) number K022569.

Who is the listed applicant for PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS?

The FDA 510(k) record lists Medical Bio Care Sweden AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS?

The FDA product code for PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS is GEX. This falls under the Gastroenterology category.

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Other records listing Medical Bio Care Sweden AB 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.

K023081PROLITE / PLASMALITE MPX PULSED LIGHT SYSTEM (PERMANENT HAIR REDUCTION)K022378PLASMALITE PULSED LIGHT SYSTEMK022568PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF UNWANTED HAIRK013365PROLITE PULSED LIGHT SYSTEM FOR THE TREATMENT OF PIGMENTED LESIONS AND THE REMOVAL OF TATTOOSK013366PROLITE PULSED LIGHT SYSTEM FOR THE REMOVAL OF UNWANTED HAIRK010927MODIFICATION TO PROLITE PULSED LIGHT 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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