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

FLOW DIRECTED THERMAL-DILUTION INFUSION

K Number: K821057 · Decision May 18, 1982
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
98
Applicant Total
12
Review Days
32

Basic Information

Device Name
FLOW DIRECTED THERMAL-DILUTION INFUSION
K Number
K821057
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1240
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
OXIMETRIX, INC.
Date Received
April 16, 1982
Decision Date
May 18, 1982
Product Code
DYG
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
DYG Catheter, Flow Directed

Similar 510(k) Clearances

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

View all

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
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. →