510(k) K051786

Device
MELIDE FIBEROPTIC LIGHT
Applicant
Designs For Vision, Inc.
510(k) number
K051786
Product code
FST
Decision
Substantially Equivalent (SESE)
Decision date
2005-08-15
Date received
2005-07-01
Regulation
878.4580
Classification name
Light, Surgical, Fiberoptic
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
CYNTHIA J M. NOLTE
Address
49 Plain St. North Attleboro MA US 02760 02760

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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