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

ACCUFIBRIN(TM) BLOOD COLLECTION SYSTEM AF100

K Number: K882501 · Decision Jul 18, 1988
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
38
Applicant Total
143
Review Days
31

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Basic Information

Device Name
ACCUFIBRIN(TM) BLOOD COLLECTION SYSTEM AF100
K Number
K882501
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1675
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Terumo Medical Corp.
Date Received
June 17, 1988
Decision Date
July 18, 1988
Product Code
GIM
Advisory Committee
Clinical Chemistry
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
GIM Tubes, Vacuum Sample, With Anticoagulant

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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. →