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

PTI INTRA-ART(TM) CORONARY ARTERY OCCLUDERS (STER)

K Number: K882879 · Decision Sep 12, 1988
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
19
Review Days
63

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Basic Information

Device Name
PTI INTRA-ART(TM) CORONARY ARTERY OCCLUDERS (STER)
K Number
K882879
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Pioneering Technologies, Inc.
Date Received
July 11, 1988
Decision Date
September 12, 1988
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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Other Clearances by Pioneering Technologies, Inc.

K Number Device Name
K922025 ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIF
K905175 PTI ANNULOPLASTY RING(STERILE)
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
K897075 PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER
Search all 19 clearances from Pioneering Technologies, Inc. →