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

ARROW RADIAL ARTERY CATHETERIZATION SET

K Number: K810675 · Decision Mar 27, 1981
Classifications
1
FEI Numbers
252
Registration Numbers
253
Same Product Code
751
Applicant Total
110
Review Days
15

Basic Information

Device Name
ARROW RADIAL ARTERY CATHETERIZATION SET
K Number
K810675
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
ARROW INTL., INC.
Date Received
March 12, 1981
Decision Date
March 27, 1981
Product Code
DQX
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
DQX Wire, Guide, Catheter

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