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

PROWLER PLUS INFUSION CATHETER

K Number: K993266 · Decision Oct 28, 1999
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
170
Applicant Total
37
Review Days
28

Basic Information

Device Name
PROWLER PLUS INFUSION CATHETER
K Number
K993266
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CORDIS NEUROVASCULAR, INC.
Date Received
September 30, 1999
Decision Date
October 28, 1999
Product Code
KRA
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
KRA Catheter, Continuous Flush

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K Number Device Name
K082324 TRUFILL DCS SYRINGE
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K071962 VASCULAR OCCLUSION SYSTEM (TRUFILL PUSHABLE COILS AND TRUPUSH COIL PUSHER)
K070279 MODIFICATION TO HYPERTRANSIT INFUSION CATHETER
K063254 THE TRUFILL DCS DETACHABLE COIL SYSTEM; THE TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM
K053197 TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM LINE EXTENSION
K043538 HYPERTRANSIT INFUSION CATHETER
K032553 TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE, ALSO KNOWN AS TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM
K030963 TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE, ALSO KNOWN AS THE TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM
K021591 PROWLER SELECT (10, 14, AND PLUS) INFUSION CATHETERS WITH AND WITHOUT PRE-SHAPED TIPS
Search all 37 clearances from CORDIS NEUROVASCULAR, INC. →