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

DUAL BALLOON EMBOLECTOMY CATHETER

K Number: K914880 · Decision Mar 16, 1992
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
73
Applicant Total
16
Review Days
138

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Basic Information

Device Name
DUAL BALLOON EMBOLECTOMY CATHETER
K Number
K914880
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ideal Medical, Inc.
Date Received
October 30, 1991
Decision Date
March 16, 1992
Product Code
DXE
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
DXE Catheter, Embolectomy

Similar 510(k) Clearances

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Other Clearances by Ideal Medical, Inc.

K Number Device Name
K944067 PEANUT WAND, MODIFICATION
K931115 HATCHER STONE-EMBOLIS EXTRACTOR
K926335 IDEAS PEANUT WAND
K922161 GRICE SOFT TISSUE BIOPSY KIT
K921922 GRICE LAPAROSCOPIC SUTURING NEEDLE
K915175 REDDICK RETRACTOR
K913602 IDEAS' PORT
K914913 GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST
K912540 CONTOUR-PORT
K911601 REDDICK TROCAR AND CANNULA
Search all 16 clearances from Ideal Medical, Inc. →