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

INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM

K Number: K972684 · Decision Oct 10, 1997
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
12
Review Days
85

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Basic Information

Device Name
INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM
K Number
K972684
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innerdyne, Inc.
Date Received
July 17, 1997
Decision Date
October 10, 1997
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DYB), ordered by most recent decision date.

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Other Clearances by Innerdyne, Inc.

K Number Device Name
K992668 INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM (REVAS)
K990854 INNERDYNE RADIALLY EXPANDING DILATION, RED DEVICE
K990493 INNERDYNE GENERIC RADIALLY EXPANDING DILATION, G-RED DEVICE
K982417 INNERDYNE STEP TROCAR EXPANDABLE PORT, STEP
K980578 INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM (HEPARIN COATED)
K971230 SHERWOOD MEDICAL COMPANY , KANGAROO, ENTRISTAR, PERCUTANEOUS GASTROSTOMY KIT
K970754 INNERDYNE STEP TROCAR EXPANABLE PORT, OPEN STEP
K961940 INNERDYNE STEP TROCAR EXPANDABLE PORT, ONESTEP
K961430 INNERDYNE STEP TROCAR EXPANDABLE PORT, MINISTEP
K950632 INNERDYNE STEP TROCAR EXPANDABLE PORT, STEP
Search all 12 clearances from Innerdyne, Inc. →