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

THE GRIPPER(TM) PORT-A-CATH NEEDLES

K Number: K870866 · Decision Jun 25, 1987
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
129
Review Days
114

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Basic Information

Device Name
THE GRIPPER(TM) PORT-A-CATH NEEDLES
K Number
K870866
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Pharmacia, Inc.
Date Received
March 3, 1987
Decision Date
June 25, 1987
Product Code
FPA
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
FPA Set, Administration, Intravascular

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