FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MACRO SUCTION TUBE MODEL NO 10061

K Number: K950754 · Decision Apr 25, 1995
Classifications
1
FEI Numbers
213
Registration Numbers
213
Same Product Code
95
Applicant Total
56
Review Days
67

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Basic Information

Device Name
MACRO SUCTION TUBE MODEL NO 10061
K Number
K950754
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dlp, Inc.
Date Received
February 17, 1995
Decision Date
April 25, 1995
Product Code
GCY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered

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K913077 LANCASTER COOLING JACKET, CAT. CODE #13500/13501
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K912229 IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003
K904172 ACCUPLACE (TM)
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