FDA 510(k), K162218, Pain Freeze™, Medium Stream Spray, Model #2101; Pain Freeze™, Mist Spray, Model #2102

FDA 510(k), K162218, Pain Freeze™, Medium Stream Spray, Model #2101; Pain Freeze™, Mist Spray, Model #2102

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510(K) Number: K162218
Device Name: Pain Freeze™, Medium Stream Spray, Model #2101; Pain Freeze™, Mist Spray, Model #2102
Manufacturer: NUANCE MEDICAL, LLC
Device Classification Name: vapocoolant device
Regulation Number:
Classification Product Code: MLY
Date Received: 08/08/2016
Decision Date: 11/22/2016
Regulation Medical Specialty:

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