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

BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM

K Number: K060277 · Decision Mar 3, 2006
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
76
Applicant Total
38
Review Days
29

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Basic Information

Device Name
BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM
K Number
K060277
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
Boehringer Laboratories
Date Received
February 2, 2006
Decision Date
March 3, 2006
Product Code
JCX
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
JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered

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K014187 AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM
K013976 BOEHRINGER MRI SUCTION REGULATORY
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K932093 AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S
K933232 BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED
K930615 AUTOVAC CLOSED WOUND SUCTION SYSTEM
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