510(k) K200037

Piccolo Medical SmartPICC System by Piccolo Medical, Inc. — Product Code LJS

K200037 is an FDA 510(k) premarket notification submitted by Piccolo Medical, Inc. for the device "Piccolo Medical SmartPICC System". The FDA issued a decision of Substantially Equivalent on January 22, 2021. The device falls under product code LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days), a Class II device regulated under 21 CFR 880.5970. Piccolo Medical, Inc. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 22, 2021
Date Received
January 8, 2020
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Device Class
Class II
Regulation Number
880.5970
Review Panel
HO
Submission Type