FDA 510(k), K961918, MULTI-TEST II
FDA 510(k), K961918, MULTI-TEST II
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$149.00 USD
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510(K) Number: K961918
Device Name: MULTI-TEST II
Manufacturer:
Device Classification Name: System, Delivery, Allergen And Vaccine
Regulation Number:
Classification Product Code: LDH
Date Received: 05/17/1996
Decision Date: 08/07/1996
Regulation Medical Specialty:
Device Name: MULTI-TEST II
Manufacturer:
Device Classification Name: System, Delivery, Allergen And Vaccine
Regulation Number:
Classification Product Code: LDH
Date Received: 05/17/1996
Decision Date: 08/07/1996
Regulation Medical Specialty: