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

PTI INTRA-ARTR REUSABLE CORONARY ARTERY PROBE

K Number: K901531 · Decision Jun 20, 1990
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
0
Applicant Total
19
Review Days
90

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Basic Information

Device Name
PTI INTRA-ARTR REUSABLE CORONARY ARTERY PROBE
K Number
K901531
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3380
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Pioneering Technologies, Inc.
Date Received
March 22, 1990
Decision Date
June 20, 1990
Product Code
DNP
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DNP Thin Layer Chromatography, Ethosuximide

Other Clearances by Pioneering Technologies, Inc.

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
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. →