FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇮 Slovenia

FOTONA NOVALIS R RUBY LASER SYSTEM

K Number: K991634 · Decision Aug 10, 1999
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
27
Review Days
90

Basic Information

Device Name
FOTONA NOVALIS R RUBY LASER SYSTEM
K Number
K991634
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
FOTONA D.D.
Date Received
May 12, 1999
Decision Date
August 10, 1999
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

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Other Clearances by FOTONA D.D.

K Number Device Name
K143723 SP Dynamis, SP Spectro, XS Dynamis, XP Dynamis, XP Spectro
K132806 FOTONA F-22 LASER HANDPIECE (F-RUNNER), FOTONA FS-01 LASER HANDPIECE
K121508 LIGHTWALKER AT LIGHTWALKER DT LIGHTWALKER ST-E LIGHTWALKER ST-N
K113702 FOTONA XP ND: YAG LASER SYSTEM
K101306 SP DYNAMIS, SP SPECTRO, XS DYNAMIS, XS SPECTRO, XP DYNAMIS, XP SPECTRO, MODELS M021-4AF/3, M002-2A
K101817 LIGHTWALKER AT, MODEL M021-5AF/1, LIGHTWALKER DT, MODEL M021-5AF/2, LIGHTWALKER ST-E, MODEL M002-6A/2, LIGHTWALKER ST-N
K093162 FIDELIS PLUS III D, AT FIDELIS D, POWERLASE AT D / FIDELIS PLUS III, AT FIDELIS, POWERLASE AT / FIDELIS ER III D, HT FID
K090126 FOTONA XP ND: YAG LASER SYSTEM FAMILY, FOTONA XP, XP-2 FOCUS, FOTONA XP CHANGER,MODEL MOO1-14F, MOO1-14F, MOO1-14F/2,
K083889 FOTONA QX ND:YAG/KTP LASER SYSTEM FAMILY
K083034 FOTONA XD-2 DIODE LASER SYSTEM, MODEL MD01-2F
Search all 27 clearances from FOTONA D.D. →