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

ALMA LASERS FAMILY OF ACCENT RADIOFREQUENCY (RF) SYSTEMS, MODELS: ACCENT, ACCENT XL

K Number: K072699 · Decision Oct 5, 2007
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
14
Review Days
11

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Basic Information

Device Name
ALMA LASERS FAMILY OF ACCENT RADIOFREQUENCY (RF) SYSTEMS, MODELS: ACCENT, ACCENT XL
K Number
K072699
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alma Lasers , Ltd.
Date Received
September 24, 2007
Decision Date
October 5, 2007
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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Other Clearances by Alma Lasers , Ltd.

K Number Device Name
K212073 Alma Diode Tabletop Laser
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K170850 Alma Q
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K140005 ALMA DIODE TABLETOP LASER
K090571 ALMA LASERS ALEX755 MODULE
K083848 ALMA LASERS SOPRANO XL MULTI-APPLICATION PLATFORM
K082622 ALMA LASERS ACCENT B-SHAPE MASSAGER HANDPIECE/MODULE
K080463 ALMA LASERS THERMOXEL CO2 LASER SYSTEM AND DELIVERY DEVICE ACCESSORIES
K072182 ALMA LASERS FAMILY OF THERMO-XEL HANDPIECES, PIXEL MODELS: 2940, 1060
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