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

EMERGE FRACTIONAL LASER

K Number: K111840 · Decision Nov 14, 2011
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
34
Applicant Total
21
Review Days
138

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Basic Information

Device Name
EMERGE FRACTIONAL LASER
K Number
K111840
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Palomar Medical Products, Inc.
Date Received
June 29, 2011
Decision Date
November 14, 2011
Product Code
ONG
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
ONG Powered Laser Surgical Instrument With MicrobeamFractional Output

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ONG), ordered by most recent decision date.

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Other Clearances by Palomar Medical Products, Inc.

K Number Device Name
K091446 MODIFICATION TO LUX1540 HANDPIECE AND LUX 1440 HANDPIECE
K092222 THERMAPULSE
K090525 LOI SYSTEM
K083900 ERBIUM FRACTIONAL HANDPIECE
K083165 PALOMAR ASPIRE LASER PLATFORM
K080244 PALOMAR LUX 1540 HANDPIECE
K081416 PALOMAR ASPIRE LASER PLATFORM
K080567 PALOMAR ASPIRE LASER PLATFORM
K073583 MODIFICATION TO PALOMAR LUX1540 HANDPIECE
K071768 ERBIUM FRACTIONAL HANDPIECE
Search all 21 clearances from Palomar Medical Products, Inc. →