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

LIPOPLASTY/ LIPOSUCTION ASPIRATION AND TUMESCENT INFUSION CANNULAE AND NEEDLES

K Number: K981172 · Decision Jun 30, 1998
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
57
Applicant Total
27
Review Days
90

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Basic Information

Device Name
LIPOPLASTY/ LIPOSUCTION ASPIRATION AND TUMESCENT INFUSION CANNULAE AND NEEDLES
K Number
K981172
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Byron Medical
Date Received
April 1, 1998
Decision Date
June 30, 1998
Product Code
QPB
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
QPB System, Suction, Lipoplasty For Removal

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K Number Device Name
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K980738 PSI-TEC SYRINGE INFUSION PUMP AND ACCESSORIES FOR GENERAL FLUID IRRIGAION/INFILTRATION
K980392 PSI-TEC ASPIRATOR
K974295 BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING
K973133 BIG BAG 3000 PRESSURE INFUSOR
K934179 DISPOSABLE BAG DECANTER
K934233 ZARA ZONE IV MALAR IMPLANT MODIFICATION
K933670 BIOPSY PUNCH, SURGICAL
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