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

PENUMBRA ASPIRATION PUMP, MODEL 115V

K Number: K051758 · Decision Aug 17, 2005
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
87
Review Days
49

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Basic Information

Device Name
PENUMBRA ASPIRATION PUMP, MODEL 115V
K Number
K051758
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Penumbra, Inc.
Date Received
June 29, 2005
Decision Date
August 17, 2005
Product Code
BTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
BTA Pump, Portable, Aspiration (Manual Or Powered)

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K Number Device Name
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K252612 INDIGO® Aspiration System – Lightning Flash Aspiration Tubing; INDIGO® Aspiration System – Lightning Bolt Aspiration Tubing
K250079 Ruby XL System
K242104 Penumbra System (Reperfusion Catheter RED 72)
K242033 Access25™ Delivery Microcatheter
K242520 Element Vascular Access System
K242075 Indigo® Aspiration System – Lightning Bolt Aspiration Tubing
K242319 Indigo® Aspiration System – Aspiration Catheter 6X
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