FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TIBIAL ARTERY CLAMP W/ATRAUGRIP JAWS

K Number: K760648 · Decision Sep 21, 1976
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
39
Review Days
6

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Basic Information

Device Name
TIBIAL ARTERY CLAMP W/ATRAUGRIP JAWS
K Number
K760648
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Pilling Co.
Date Received
September 15, 1976
Decision Date
September 21, 1976
Product Code
DWS
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
DWS Instruments, Surgical, Cardiovascular

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K911099 MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE
K911100 MEHIGAN-PILLING PHLEBETOME TM
K904507 PILLING BRUSH VALVULOTOME
K884946 JEHLE CORONARY PERFUSION CATHETERS
K882930 LASER LARYNGOSCOPE DEDO ARTICULA. & FEDER DEDO EX
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