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

SMARTSUCTION SOLO DEVICE

K Number: K062801 · Decision Oct 4, 2006
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
28
Review Days
15

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Basic Information

Device Name
SMARTSUCTION SOLO DEVICE
K Number
K062801
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Haemonetics Corp.
Date Received
September 19, 2006
Decision Date
October 4, 2006
Product Code
BTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BTA Pump, Portable, Aspiration (Manual Or Powered)

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Other Clearances by Haemonetics Corp.

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K061103 HAEMONETICS 40U RBC FILTER BAG
K053000 HAEMONETICS CARDIOVASCULAR PERIOPERATIVE AUTOTRANSFUSION SYSTEM (CARDIOPAT)
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
K953681 HAEMONETICS THERAPEUTIC PLASMA EXCHANGE SET
Search all 28 clearances from Haemonetics Corp. →