FDA 510(k), K942901, SHARPS-TAINER LARGE OPENING

FDA 510(k), K942901, SHARPS-TAINER LARGE OPENING

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510(K) Number: K942901
Device Name: SHARPS-TAINER LARGE OPENING
Manufacturer:
Device Classification Name: Needle, Hypodermic, Single Lumen
Regulation Number: 880.5570
Classification Product Code: FMI
Date Received: 04/28/1994
Decision Date: 09/19/1994
Regulation Medical Specialty: General Hospital
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