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

CERALAS D 980NM DIODE LASER, MODELS D15 AND D25

K Number: K072779 · Decision Jan 24, 2008
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
28
Review Days
118

Basic Information

Device Name
CERALAS D 980NM DIODE LASER, MODELS D15 AND D25
K Number
K072779
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
BIOLITEC, INC.
Date Received
September 28, 2007
Decision Date
January 24, 2008
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

Similar 510(k) Clearances

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

View all

Other Clearances by BIOLITEC, INC.

K Number Device Name
K112013 EVOLVE(R) HPD 980/1470NM MULTIWAVELENGTH DIODE LASER
K112253 CERALAS 147NM DIODE LASER SYSTEM
K110080 RADIAL-EMITTING SHAPED FIBER OPTIC DELIVERY SYSTEM
K102755 CERALAS E/ 1470NM FIBER-COUPLED DIODE LASER FAMILY; CREALAS HPD MULTIWAVELENGHT 980NM/ 1470NM FIBER-COUPLED DIODE LASER
K101712 ENDOVASCULAR LAER VEIN SYSTEM KIT
K100726 CERALAS D/ 980NM FIBER-COUPLED DIODE LASER FAMILY, CERALAS E/ 980NM FIBER-COUPLED DIODE LASER FAMILY, CERALAS HPD/ 980NM
K090164 CERALAS MULTIWAVELENGTH 980/1470NM DIODE LASER
K083682 180W CERELAS D 980NM DIODE LASER, MODEL D180
K082225 15W CERALAS D 1470NM DIODE LASER, MODEL D1470
K082263 CERALAS E 980NM DIODE LASER, MODELS E15/980 AND E30/980
Search all 28 clearances from BIOLITEC, INC. →