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

Triton Canister System

K Number: K142801 · Decision Mar 12, 2015
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
5
Applicant Total
6
Review Days
164

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Basic Information

Device Name
Triton Canister System
K Number
K142801
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2750
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gauss Surgical, Inc.,
Date Received
September 29, 2014
Decision Date
March 12, 2015
Product Code
PBZ
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
PBZ Image Processing Device For Estimation Of External Blood Loss

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K Number Device Name
K163507 Triton Sponge System
K160338 Triton System
DEN130015 PIXEL 3 SYSTEM
K121274 PIXEL APP
K120473 PIXEL APP