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

CERALAS D10 810NM DIODE LASER

K Number: K992773 · Decision Sep 1, 1999
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
29
Review Days
14

Basic Information

Device Name
CERALAS D10 810NM DIODE LASER
K Number
K992773
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
CERAMOPTEC, INC.
Date Received
August 18, 1999
Decision Date
September 1, 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 CERAMOPTEC, INC.

K Number Device Name
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K993828 CERALAS D10 810NM DIODE LASER
K993911 CERALAS D DIODE LASER SYSTEM, MODEL D15, D25,D50
K993002 CERALAS D 980NM DIODE LASER SYSTEM, MODEL D15
K991891 CERALAS DIODE LASER SYSTEM, MODEL CERALAS D15
K983950 CERALAS DIODE LASER SYSTEM (MODEL H)
K983058 CERALAS D LASER SYSTEM, MODEL # CERALAS D15
K980389 MEGABEAM REUSABLE FIBER OPTIC HANDPIECE AND NEEDLES
K981126 CERALAS G FREQUENCY DOUBLED ND: YAG LASER SYSTEMS, CERALAS G3
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