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

ACCENT

K Number: K070004 · Decision Apr 23, 2007
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
11
Review Days
110

Basic Information

Device Name
ACCENT
K Number
K070004
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ALMA LASERS LTD.
Date Received
January 3, 2007
Decision Date
April 23, 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.

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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
K072564 ALMA LASERS HARMONY XL MULTI-APPLICATION PLATFORM
K080318 ALMA LASER NIR MODULE
K072699 ALMA LASERS FAMILY OF ACCENT RADIOFREQUENCY (RF) SYSTEMS, MODELS: ACCENT, ACCENT XL
Search all 11 clearances from ALMA LASERS LTD. →