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

CARDIAC OUTPUT COMPUTER

K Number: K831407 · Decision Oct 14, 1983
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
176
Applicant Total
16
Review Days
165

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
CARDIAC OUTPUT COMPUTER
K Number
K831407
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1435
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Ziehm International, Inc.
Date Received
May 2, 1983
Decision Date
October 14, 1983
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 Ziehm International, Inc.

K Number Device Name
K011292 ZIEHM VISION
K910455 IMS DISPOSABLE HOLDER WITH NEEDLE RETRACTOR
K902196 MODIFIED STICK-GARD SAFETY NEEDLE
K894021 MOBILE X-RAY UNIT
K894041 PUMP-JECT SYRINGE WITH LUER-LOCK
K890620 STICK-GARD SAFETY NEEDLE
K882133 MAMMO M
K843311 IV ADMIN. SET FOR MVP 1 INFUSION PUMP
K842263 MTP E.V. INFUSION PUMP
K830453 IV ADMINISTRATION SETS - MVP INFUSION
Search all 16 clearances from Ziehm International, Inc. →