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

MODEL 3000 OPTICATH COMPUTER

K Number: K853018 · Decision Jan 13, 1986
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
176
Applicant Total
12
Review Days
180

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Basic Information

Device Name
MODEL 3000 OPTICATH COMPUTER
K Number
K853018
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1435
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Oximetrix, Inc.
Date Received
July 17, 1985
Decision Date
January 13, 1986
Product Code
DXG
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DXG Computer, Diagnostic, Pre-Programmed, Single-Function

Similar 510(k) Clearances

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

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Other Clearances by Oximetrix, Inc.

K Number Device Name
K842622 HEMO STATIC/ESU SCALPEL SYSTEM
K833966 PUMP INFUSION WEARABLE INFUSION PUMP
K823007 OPTICATH HEPARIN COATED, FLOW-DIRECT
K821056 FLOW DIRECTED THERMAL-DILUTION CATHETER
K821057 FLOW DIRECTED THERMAL-DILUTION INFUSION
K820674 OPTICATH
K811391 OXIMETRIX ACCU SAT CPB
K791868 OXIMETRIX SHAW HEMOSTATIC SURG. SYS.
K781879 HEATER, OXIMETER SYSTEM
K781134 CATHETER, THERMAL DILUTION FIBEROPTIC
Search all 12 clearances from Oximetrix, Inc. →