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

DETACHABLE SILICONE BALLOON (DSB)

K Number: K964488 · Decision Apr 21, 1998
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
1
Applicant Total
70
Review Days
529

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Basic Information

Device Name
DETACHABLE SILICONE BALLOON (DSB)
K Number
K964488
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5950
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Target Therapeutics
Date Received
November 8, 1996
Decision Date
April 21, 1998
Product Code
MZQ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MZQ Balloon, Detachable, For Neurovascular Occlusion

Similar 510(k) Clearances

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

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Other Clearances by Target Therapeutics

K Number Device Name
K965071 DETACHABLE SLICONE BALLOON (DSB)
K964210 RETRIEVER II
K971395 GUGLIELMI DETACHABLE COIL (GDC), FIBERED PLATINUM COIL, .035 TYPE, BERENSTEIN LIQUID COIL, FIBERED PLATINUM COILS, ACCE
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
Search all 70 clearances from Target Therapeutics →