Atlas FDA

1424 TUMISTORE

FDA 510(k) clearance K822914 · decided 1982-12-03

Clearance details

K-number
K822914
Device name
1424 TUMISTORE
Applicant
Life-Tech Intl., Inc.
Decision
Substantially Equivalent
Date received
1982-10-01
Decision date
1982-12-03
Days to decision
63 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Walker, MI, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.