Atlas FDA

OCULAR PRESSURE APPLICATOR

FDA 510(k) clearance K841652 · decided 1984-06-01

Clearance details

K-number
K841652
Device name
OCULAR PRESSURE APPLICATOR
Applicant
The Lebanon Corp.
Decision
Substantially Equivalent
Date received
1984-04-20
Decision date
1984-06-01
Days to decision
42 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.