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

PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER

K Number: K897075 · Decision Apr 10, 1990
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
19
Review Days
111

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Basic Information

Device Name
PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER
K Number
K897075
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Pioneering Technologies, Inc.
Date Received
December 20, 1989
Decision Date
April 10, 1990
Product Code
DXC
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
DXC Clamp, Vascular

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K Number Device Name
K922025 ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIF
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K905068 PTI INTRA-ART (TM) PICK-UP WICKS
K910067 PTI STERNAL CLOSURE WIRE SUTURE
K905067 PTI ANASTOMARK FLEXIBLE CORONARY BYPASS GRAFT
K901815 MODIFIED STERILIZATION OF INTRA-ART(TM) CORONARY
K901682 PTI ANASTOMARK(TM) CORONARY BYPASS GRAFT MARKERS
K901531 PTI INTRA-ARTR REUSABLE CORONARY ARTERY PROBE
K901575 REUSABLE TENS PARAVERTEBRAL PAD #641 BACK ELECTROD
K894684 PTI INTRA-ART INTERNAL MAMMARY ARTERY CANNULA KIT
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