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

TRIAL LENS SET

K Number: K821082 · Decision Jun 14, 1982
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
1
Applicant Total
13
Review Days
56

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Basic Information

Device Name
TRIAL LENS SET
K Number
K821082
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1700
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Medical Equipment Designs, Inc.
Date Received
April 19, 1982
Decision Date
June 14, 1982
Product Code
HLH
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
HLH Pupillometer, Manual

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Other Clearances by Medical Equipment Designs, Inc.

K Number Device Name
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K894152 MEDITHERM
K895375 MULTISPIRO
K851277 MICROSPIRO-SDS
K840908 CHESTAC-25F SPIROMETER
K840929 FRC 85 SERIES SPIROMETER
K821081 CHART PROJECTOR
K821084 UNIVERSAL TRIAL FRAMEE
K821107 EXOPHTHALMOMETER
K821083 P.D. METER
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