FDA 510(k), K052099, NASOPORE NASAL DRESSING, MODEL NDOX-YYY/ZZ

FDA 510(k), K052099, NASOPORE NASAL DRESSING, MODEL NDOX-YYY/ZZ

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510(K) Number: K052099
Device Name: NASOPORE NASAL DRESSING, MODEL NDOX-YYY/ZZ
Manufacturer: JAN NIEUWENHUIS
Device Classification Name: Splint, Intranasal Septal
Regulation Number: LYA
Classification Product Code: 08/03/2005
Date Received: 11/21/2005
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ear Nose & Throat
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