FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AUTOREFRACTOR, SUBJECTIVE

K Number: K781014 · Decision Sep 7, 1978
Classifications
1
FEI Numbers
74
Registration Numbers
75
Same Product Code
34
Applicant Total
32
Review Days
83

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Basic Information

Device Name
AUTOREFRACTOR, SUBJECTIVE
K Number
K781014
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1760
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Cavitron Corp.
Date Received
June 16, 1978
Decision Date
September 7, 1978
Product Code
HKO
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
HKO Refractometer, Ophthalmic

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K800722 AUTO-FIELD D AUTOMATED VISUAL DETECTOR
K791585 MODEL G-61 ULTRASONIC DENTAL UNIT
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