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

HAEMONETICS 170 Y INFUSION SET

K Number: K810365 · Decision Mar 31, 1981
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
28
Review Days
47

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Basic Information

Device Name
HAEMONETICS 170 Y INFUSION SET
K Number
K810365
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Haemonetics Corp.
Date Received
February 12, 1981
Decision Date
March 31, 1981
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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K052626 SMARTSUCTION HARMONY DEVICE
K043127 HAEMONETICS CARDIOVASCULAR PERIOPERATIVE AUTOTRANSFUSION SYSTEM
K014083 HAEMONETICS CELL SAVER 5 AUTOLOGOUS BLOOD RECOVERY SYSTEM
K993581 HAEMONETICS LN 193 DISPOSABLE SET, FOR USE WITH THE HAEMONETICS CELLSEVER HAEMOLITE 2 FAMILY OF AUTOLOGOUS BLOOD RECOVER
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