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

PAL System

K Number: K212024 · Decision Jun 10, 2022
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
57
Applicant Total
9
Review Days
346

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Basic Information

Device Name
PAL System
K Number
K212024
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
Microaire Surgical Instruments, LLC
Date Received
June 29, 2021
Decision Date
June 10, 2022
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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K242804 PAL Aspiration System
K220318 PAL Infiltration System
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K171286 PAL Multi-Use Cannulas and PAL Manual Wand
K150779 LipoFilter - Hospital Pack, LipoFilter - Clinic Pack
K113128 MICROAIRE SURGICAL INSTRUMENTS LLC