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510(k) K030081

CSF400 AND CSF600 by Inmed Ltda. — Product Code JXG

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 6, 2003
Date Received
January 9, 2003
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Shunt, Central Nervous System And Components
Device Class
Class II
Regulation Number
882.5550
Review Panel
NE
Submission Type

Other clearances by Inmed Ltda.

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  • K030889 — ULTRAEKOGEL MODELS EK 2000 & EK 2001 (May 23, 2003)

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