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

UNIVERSAL TRIAL FRAMEE

K Number: K821084 · Decision Jun 14, 1982
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
4
Applicant Total
13
Review Days
56

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Basic Information

Device Name
UNIVERSAL TRIAL FRAMEE
K Number
K821084
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1415
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Medical Equipment Designs, Inc.
Date Received
April 19, 1982
Decision Date
June 14, 1982
Product Code
HPA
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
HPA Frame, Trial, Ophthalmic

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K851277 MICROSPIRO-SDS
K840908 CHESTAC-25F SPIROMETER
K840929 FRC 85 SERIES SPIROMETER
K821081 CHART PROJECTOR
K821107 EXOPHTHALMOMETER
K821083 P.D. METER
K821082 TRIAL LENS SET
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