Atlas FDA

OFTALMOGRAF

FDA 510(k) clearance K833024 · decided 1984-04-26

Clearance details

K-number
K833024
Device name
OFTALMOGRAF
Applicant
Universal Instruments Corp.
Decision
Substantially Equivalent
Date received
1983-09-06
Decision date
1984-04-26
Days to decision
233 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.