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

TERUMO SURGUARD SAFETY SYRINGE

K Number: K024249 · Decision Feb 21, 2003
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
161
Applicant Total
143
Review Days
60

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Basic Information

Device Name
TERUMO SURGUARD SAFETY SYRINGE
K Number
K024249
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Terumo Medical Corp.
Date Received
December 23, 2002
Decision Date
February 21, 2003
Product Code
MEG
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
MEG Syringe, Antistick

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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
K082997 TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER
K090040 RADIFOCUS GLIDECATH (OR RADIFOCUS GLIDECATH XP)
K082847 PINNACLE ROII INTRODUCER SHEATH
K082519 FINECROSS MG CORONARY MICRO-GUIDE CATHETER
K082736 RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER
Search all 143 clearances from Terumo Medical Corp. →