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

ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIF

K Number: K922025 · Decision Sep 22, 1992
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
187
Applicant Total
19
Review Days
168

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Basic Information

Device Name
ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIF
K Number
K922025
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pioneering Technologies, Inc.
Date Received
April 7, 1992
Decision Date
September 22, 1992
Product Code
DSY
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
DSY Prosthesis, Vascular Graft, Of 6mm And Greater Diameter

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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
K897075 PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER
K894684 PTI INTRA-ART INTERNAL MAMMARY ARTERY CANNULA KIT
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