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Acculaser, Inc.

2 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
ACCULASER PRO4 (K023060)Acculaser, Inc.2004-03-19
ACCULASER PRO LOW LEVEL LASER THERAPY DEVICE (K020657)Acculaser, Inc.2002-07-29

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Every clearance here is in the API, with alerts when new ones post.