Atlas FDA

CONCORD CARE TRAY

FDA 510(k) clearance K862039 · decided 1986-07-03

Clearance details

K-number
K862039
Device name
CONCORD CARE TRAY
Applicant
Concord Laboratories, Inc.
Decision
Unknown
Date received
1986-05-28
Decision date
1986-07-03
Days to decision
36 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Keene, NH, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.