FDA 510(k), K981318, DUAL LUER LOCK CAP
FDA 510(k), K981318, DUAL LUER LOCK CAP
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$149.00 USD
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510(K) Number: K981318
Device Name: DUAL LUER LOCK CAP
Manufacturer:
Device Classification Name: Set, Administration, Intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 04/10/1998
Decision Date: 04/22/1998
Regulation Medical Specialty: General Hospital
Device Name: DUAL LUER LOCK CAP
Manufacturer:
Device Classification Name: Set, Administration, Intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 04/10/1998
Decision Date: 04/22/1998
Regulation Medical Specialty: General Hospital