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

TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER

K Number: K082997 · Decision Apr 15, 2009
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
143
Review Days
189

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Basic Information

Device Name
TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER
K Number
K082997
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Terumo Medical Corp.
Date Received
October 8, 2008
Decision Date
April 15, 2009
Product Code
FOZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
Y

Classifications

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

Product Code Device Name
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Similar 510(k) Clearances

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

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Other Clearances by Terumo Medical Corp.

K Number Device Name
K111606 PINNACLE PRECISION ACCESS SYSTEM
K111556 GLIDECROSS SUPPORT CATHETER
K110540 TERUMO SUPPORT CATHETER
K102008 GLIDESHEATH
K091329 PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH
K090040 RADIFOCUS GLIDECATH (OR RADIFOCUS GLIDECATH XP)
K082847 PINNACLE ROII INTRODUCER SHEATH
K082519 FINECROSS MG CORONARY MICRO-GUIDE CATHETER
K082736 RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER
K082644 GLIDESHEATH
Search all 143 clearances from Terumo Medical Corp. →