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

IVT INTRODUCER SHEATH

K Number: K903463 · Decision Jan 3, 1991
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
12
Review Days
155

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Basic Information

Device Name
IVT INTRODUCER SHEATH
K Number
K903463
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Intensive Technology, Inc.
Date Received
August 1, 1990
Decision Date
January 3, 1991
Product Code
DYB
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
DYB Introducer, Catheter

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Other Clearances by Intensive Technology, Inc.

K Number Device Name
K922970 INTRA-OPERATIVE TEC ATHERECTOMY SYSTEM
K912664 TEC ROTATING DUAL HEMOVALVE
K911869 IVT GUIDING CATHETER
K904003 HEMOCHRON(R) HEPARIN RESPONSE TEST
K901767 MODIFIED IVT PERIPHERAL ATHERECTOMY
K896403 MODIFIED IVT PERIPHERAL ATHERECTOMY SYSTEM
K895903 IVT 0.014 GUIDE WIRE
K892209 APTT BY HEMOCHRON(R)
K890515 PERIPHERAL ATHERECTOMY SYSTEM
K882804 0.014 PERIPHERAL GUIDE WIRE
Search all 12 clearances from Intensive Technology, Inc. →