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

GLIDESHEATH

K Number: K033681 · Decision Dec 11, 2003
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
21
Review Days
17

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Basic Information

Device Name
GLIDESHEATH
K Number
K033681
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Terumo Corp.
Date Received
November 24, 2003
Decision Date
December 11, 2003
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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K090973 TERUMO SURSHIELD SAFETY I.V. CATHETER (18G X 51MM & 20G X 51MM SIZES)
K073474 CAPIOX CIRCUIT CONNECTORS
K071572 CAPIOX FX05 HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER
K071494 CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR AND ARTERIAL FILTER
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K040783 FOUNDATION
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