Atlas FDA

URINARY DIVERSION STENT

FDA 510(k) clearance K830803 · decided 1983-05-05

Clearance details

K-number
K830803
Device name
URINARY DIVERSION STENT
Applicant
Van-Tec, Inc.
Decision
Substantially Equivalent
Date received
1983-03-14
Decision date
1983-05-05
Days to decision
52 days
Clearance type
Traditional
Product code
LJE
Device class
U
Medical specialty
Unknown
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.