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

CHASE VESSEL OCCLUDER

K Number: K964390 · Decision Jan 31, 1997
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
89
Applicant Total
27
Review Days
88

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Basic Information

Device Name
CHASE VESSEL OCCLUDER
K Number
K964390
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Chase Medical, Inc.
Date Received
November 4, 1996
Decision Date
January 31, 1997
Product Code
MJN
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
MJN Catheter, Intravascular Occluding, Temporary

Similar 510(k) Clearances

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

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Other Clearances by Chase Medical, Inc.

K Number Device Name
K032531 CHASE CARDIAC ANALYSIS SYSTEM
K022093 CHASE CARDIOVASCULAR PATCH KIT
K021129 CHARE CARIOVASCULAR PATCH
K020233 CHASE CARDIOVASCULAR PATCH KIT
K020132 CHASE CARDIOVASCULAR PATCH KIT
K012248 CHASE CARDIOVASCULAR PATCH
K003467 CHASE CARDIOVASCULAR PATCH
K001662 CHASE CARDIOVASCULAR PATCH
K972993 CHASE FEMORAL ACCESS CANNULATION SET
K974568 CHASE ANASTOMOSIS VISUALIZATION DEVICE
Search all 27 clearances from Chase Medical, Inc. →