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

OPTICATH

K Number: K820674 · Decision Mar 25, 1982
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
18
Applicant Total
12
Review Days
14

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Basic Information

Device Name
OPTICATH
K Number
K820674
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1230
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Oximetrix, Inc.
Date Received
March 11, 1982
Decision Date
March 25, 1982
Product Code
DQE
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
DQE Catheter, Oximeter, Fiber-Optic

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Other Clearances by Oximetrix, Inc.

K Number Device Name
K853018 MODEL 3000 OPTICATH COMPUTER
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
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. →