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

RETRIEVER II

K Number: K964210 · Decision Oct 31, 1997
Classifications
1
FEI Numbers
210
Registration Numbers
211
Same Product Code
499
Applicant Total
70
Review Days
374

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Basic Information

Device Name
RETRIEVER II
K Number
K964210
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1200
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Target Therapeutics
Date Received
October 22, 1996
Decision Date
October 31, 1997
Product Code
DQO
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
DQO Catheter, Intravascular, Diagnostic

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K965189 SPINNAKER
K964112 BERENSTEIN COIL
K963307 GDC PATIENT RETURN ELECTTRODE MODEL 45021
K962503 GUGLIELMI DETACHABLE COIL
K961923 BERENSTEIN COIL
K960705 GUGLIELMI DETACHABLE COIL
K960806 TURBO TRACKER
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