FDA 510(k), K111763, PATHASSIST LIGHT FIBER
FDA 510(k), K111763, PATHASSIST LIGHT FIBER
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$149.00 USD
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510(K) Number: K111763
Device Name: PATHASSIST LIGHT FIBER
Manufacturer:
Device Classification Name: Instrument, Ent Manual Surgical
Regulation Number: 874.4420
Classification Product Code: LRC
Date Received: 06/23/2011
Decision Date: 09/15/2011
Regulation Medical Specialty: Ear Nose & Throat
Device Name: PATHASSIST LIGHT FIBER
Manufacturer:
Device Classification Name: Instrument, Ent Manual Surgical
Regulation Number: 874.4420
Classification Product Code: LRC
Date Received: 06/23/2011
Decision Date: 09/15/2011
Regulation Medical Specialty: Ear Nose & Throat