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

MODIFIED STERILIZATION OF INTRA-ART(TM) CORONARY

K Number: K901815 · Decision Jul 3, 1990
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
103
Applicant Total
19
Review Days
71

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Basic Information

Device Name
MODIFIED STERILIZATION OF INTRA-ART(TM) CORONARY
K Number
K901815
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1310
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Pioneering Technologies, Inc.
Date Received
April 23, 1990
Decision Date
July 3, 1990
Product Code
DRE
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
DRE Dilator, Vessel, For Percutaneous Catheterization

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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
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
Search all 19 clearances from Pioneering Technologies, Inc. →