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

OPHTHALMOSCOPE, BINOCULAR, INDIRECT

K Number: K772214 · Decision Dec 13, 1977
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
86
Applicant Total
86
Review Days
11

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Basic Information

Device Name
OPHTHALMOSCOPE, BINOCULAR, INDIRECT
K Number
K772214
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Varian Assoc., Inc.
Date Received
December 2, 1977
Decision Date
December 13, 1977
Product Code
HLI
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
HLI Ophthalmoscope, Ac-Powered

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