FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

DESERET THERMODILUTION CARDIAC OUTPUT

K Number: K841967 · Decision Aug 19, 1985
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
176
Applicant Total
47
Review Days
461

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DESERET THERMODILUTION CARDIAC OUTPUT
K Number
K841967
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1435
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Parke-Davis Co.
Date Received
May 15, 1984
Decision Date
August 19, 1985
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.

View all

Other Clearances by Parke-Davis Co.

K Number Device Name
K861725 INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT
K862119 DESERET FLO-THRU INJECTATE TEMPERATURE SENSOR
K855120 ATI DISPOSABLE BIOLOGICAL TEST PACK
K860570 ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE
K860290 VIAPIC CENTRAL LINE CATHETER
K852192 DISPOSABLE STEAM BIOLOGICAL TEST PACK
K851327 DESERET ARTERIAL CATHETER
K852078 SPECTRUM(TENTATIVE)
K844840 DESERET INTRODUCER SET
K850505 DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER
Search all 47 clearances from Parke-Davis Co. →