FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Tablo Cartridge

K Number: K210782 · Decision Nov 26, 2021
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
76
Applicant Total
9
Review Days
255

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Basic Information

Device Name
Tablo Cartridge
K Number
K210782
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Outset Medical, Inc.
Date Received
March 16, 2021
Decision Date
November 26, 2021
Product Code
FJK
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

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Other Clearances by Outset Medical, Inc.

K Number Device Name
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K232776 Tablo® Hemodialysis System; TabloCart™ with Prefiltration Drawer
K233335 Tablo® Hemodialysis System
K223248 Tablo® Hemodialysis System
K211370 Tablo Hemodialysis System
K200741 Tablo Hemodialysis System
K190793 Tablo Hemodialysis System, Tablo Cartridge
K160881 Tablo Console