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510(k) K904667

NA NEEDLES by Olympus Corp. — Product Code GDM

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 12, 1990
Date Received
October 15, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Aspiration And Injection, Reusable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type

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  • K903747 — ISLAM STERNAL PUNCTURE NEEDLE, CAT # AG-592-00-U (October 31, 1990)
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