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

MS401097-17,MS722-K,MS720,MS721,MS722

K Number: K962767 · Decision Jul 3, 1997
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
46
Applicant Total
39
Review Days
352

Basic Information

Device Name
MS401097-17,MS722-K,MS720,MS721,MS722
K Number
K962767
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ALEXANDER MFG. CO.
Date Received
July 16, 1996
Decision Date
July 3, 1997
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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