Atlas FDA

OCUTOME PARATUBING SET

FDA 510(k) clearance K832938 · decided 1983-10-19

Clearance details

K-number
K832938
Device name
OCUTOME PARATUBING SET
Applicant
Vxtra Corp.
Decision
Substantially Equivalent
Date received
1983-09-02
Decision date
1983-10-19
Days to decision
47 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.