510(k) K781134

CATHETER, THERMAL DILUTION FIBEROPTIC by Oximetrix, Inc. — Product Code DQE

K781134 is an FDA 510(k) premarket notification submitted by Oximetrix, Inc. for the device "CATHETER, THERMAL DILUTION FIBEROPTIC". The FDA issued a decision of Substantially Equivalent on August 17, 1978. The device falls under product code DQE (Catheter, Oximeter, Fiber-Optic), a Class II device regulated under 21 CFR 870.1230. Oximetrix, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 17, 1978
Date Received
July 6, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Oximeter, Fiber-Optic
Device Class
Class II
Regulation Number
870.1230
Review Panel
CV
Submission Type