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

AUTO-FIELD D AUTOMATED VISUAL DETECTOR

K Number: K800722 · Decision Apr 29, 1980
Classifications
1
FEI Numbers
66
Registration Numbers
67
Same Product Code
40
Applicant Total
32
Review Days
28

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Basic Information

Device Name
AUTO-FIELD D AUTOMATED VISUAL DETECTOR
K Number
K800722
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1605
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Cavitron Corp.
Date Received
April 1, 1980
Decision Date
April 29, 1980
Product Code
HPT
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
HPT Perimeter, Automatic, Ac-Powered

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