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FDA 510(k), K833182, APLICARE ALCOHOL PREP PAD
FDA 510(k), K833182, APLICARE ALCOHOL PREP PAD
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510(K) Number: K833182
Device Name: APLICARE ALCOHOL PREP PAD
Manufacturer:
Device Classification Name: Pad, Alcohol, Device Disinfectant
Regulation Number: LKB
Classification Product Code: KXA
Date Received: 09/19/1983
Decision Date: 10/27/1983
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: APLICARE ALCOHOL PREP PAD
Manufacturer:
Device Classification Name: Pad, Alcohol, Device Disinfectant
Regulation Number: LKB
Classification Product Code: KXA
Date Received: 09/19/1983
Decision Date: 10/27/1983
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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