FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

Rapid Barostat Bag (RBB) Pump and Catheter

K Number: K160287 · Decision Mar 14, 2017
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
68
Applicant Total
4
Review Days
405

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Basic Information

Device Name
Rapid Barostat Bag (RBB) Pump and Catheter
K Number
K160287
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1725
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mui Scientific
Date Received
February 3, 2016
Decision Date
March 14, 2017
Product Code
FFX
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
FFX System, Gastrointestinal Motility (Electrical)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FFX), ordered by most recent decision date.

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Other Clearances by Mui Scientific

K Number Device Name
K122294 PRESSURIZED INFUSION PUMP
K120524 SPHINCTER OF ODDI MANOMETRIC (SOM) SYSTEM
K823701 MOTILITY CATHETERS