FDA 510(k), K113808, THE SHERLOCK 3CG TIP CONFIRMATION SYSTEM (TCS)
FDA 510(k), K113808, THE SHERLOCK 3CG TIP CONFIRMATION SYSTEM (TCS)
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510(K) Number: K113808
Device Name: THE SHERLOCK 3CG TIP CONFIRMATION SYSTEM (TCS)
Manufacturer: HENRY BOLAND
Device Classification Name: Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Regulation Number: LJS
Classification Product Code: 12/23/2011
Date Received: 03/19/2012
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: THE SHERLOCK 3CG TIP CONFIRMATION SYSTEM (TCS)
Manufacturer: HENRY BOLAND
Device Classification Name: Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Regulation Number: LJS
Classification Product Code: 12/23/2011
Date Received: 03/19/2012
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital