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PULSTAR — Lasermed, Inc. (510(k) K992061)

PULSTAR — Lasermed, Inc. (510(k) K992061) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: PULSTAR; Applicant: Lasermed, Inc.; Clearance track: 510(k).

Device namePULSTAR
ApplicantLasermed, Inc.
Clearance track510(k)
Submission numberK992061
DecisionSubstantially Equivalent
Decision date1999-07-30
Date received1999-06-18
Product codeGEX
Device class2
Medical specialtyGeneral, Plastic Surgery
Applicant locationUT, US
SourceopenFDA device

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