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

PL 20/20 INFANT VISION TESTER

K Number: K883337 · Decision Oct 31, 1988
Classifications
1
FEI Numbers
106
Registration Numbers
107
Same Product Code
31
Applicant Total
15
Review Days
83

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Basic Information

Device Name
PL 20/20 INFANT VISION TESTER
K Number
K883337
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Optimed Technologies, Inc.
Date Received
August 9, 1988
Decision Date
October 31, 1988
Product Code
HOX
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
HOX Chart, Visual Acuity

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K943598 FLEXIBLE FIBER OPTIC LAPAROSCOPES
K926597 LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)
K921942 HYSTEROSCOPE (AND ACCESSORIES)
K922711 FLEXIBLE FIBER OPTIC GYNECOLOGIC ENDOSCOPE
K921985 ARTHROSCOPE & ACCESSORIES
K922826 FLEXIBLE FIBER OPTIC ENDOSCOPE
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