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

INTRA-AORTIC BALLOON PUMP CATHETER - MODIFICATION

K Number: K923603 · Decision Mar 8, 1993
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
57
Review Days
249

Basic Information

Device Name
INTRA-AORTIC BALLOON PUMP CATHETER - MODIFICATION
K Number
K923603
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KONTRON INSTRUMENTS, INC.
Date Received
July 2, 1992
Decision Date
March 8, 1993
Product Code
DYB
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
DYB Introducer, Catheter

Similar 510(k) Clearances

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

View all

Other Clearances by KONTRON INSTRUMENTS, INC.

K Number Device Name
K932268 MODIFICATIONS TO INTRA-AORTIC BALLOONS
K925248 MODIFICATION OF INTRA-AORTIC BALLOON CATHETERS
K905313 KONTRON INTRA-AORTIC BALLOON PUMP, MODEL KAAT II
K903344 9.5 FR PERCUTANEOUS DB LUMEN 40CC FLEXI-CATH (TM)
K896437 KONTRON SIGMA 44 HVCD ULTRASOUND IMAGING SYSTEM
K892222 9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOON
K882955 SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283
K896386 MINIMON 7133B PATIENT MONITOR
K896417 KONTRON KOLORMON 7250 PATIENT MONITOR
K895425 MINIMON 7137B PATIENT MONITOR
Search all 57 clearances from KONTRON INSTRUMENTS, INC. →