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

OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITS

K Number: K093495 · Decision Nov 19, 2010
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
46
Applicant Total
39
Review Days
374

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Basic Information

Device Name
OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITS
K Number
K093495
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
American Diagnostic Corp.
Date Received
November 10, 2009
Decision Date
November 19, 2010
Product Code
HLJ
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HLJ Ophthalmoscope, Battery-Powered

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