Atlas FDA

C-LOOPS

FDA 510(k) clearance K833856 · decided 1984-02-04

Clearance details

K-number
K833856
Device name
C-LOOPS
Applicant
Concept, Inc.
Decision
Substantially Equivalent
Date received
1983-11-07
Decision date
1984-02-04
Days to decision
89 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.

PMA approvals by this applicant

RecordFirmDate
HUNTER-SESSIONS VENA-CAVA OCCLUDER (P770005)Concept, Inc.1977-12-19