510(k) K904667

NA NEEDLES by Olympus Corp. — Product Code GDM

K904667 is an FDA 510(k) premarket notification submitted by Olympus Corp. for the device "NA NEEDLES". The FDA issued a decision of Substantially Equivalent on December 12, 1990. The device falls under product code GDM (Needle, Aspiration And Injection, Reusable), a Class I device regulated under 21 CFR 878.4800. Olympus Corp. has at least 10 other 510(k) clearances on record.

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