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

SAFE-CONNECT Y-SITE ADAPTER CATALOG NO. 681518

K Number: K971266 · Decision May 1, 1997
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
6
Review Days
27

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Basic Information

Device Name
SAFE-CONNECT Y-SITE ADAPTER CATALOG NO. 681518
K Number
K971266
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Faulding Medical Device Co.
Date Received
April 4, 1997
Decision Date
May 1, 1997
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FPA), ordered by most recent decision date.

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Other Clearances by Faulding Medical Device Co.

K Number Device Name
K962159 STERILE AMBULATORY RESERVOIR 60ML/100ML
K970909 SAFE-CONNECT I.V. SET
K970789 SAFE-CONNECT VIAL DISPENSING SPIKE
K970524 SAFE-CONNECT I.V. EXTENSION SET
K955775 SAFECONNECT VALVE (CATALOG NO. XXXX)