510(k) K974741

MANAN ACCURA NEEDLE by Medical Device Technologies, Inc. — Product Code GAA

K974741 is an FDA 510(k) premarket notification submitted by Medical Device Technologies, Inc. for the device "MANAN ACCURA NEEDLE". The FDA issued a decision of Substantially Equivalent on January 8, 1998. The device falls under product code GAA (Needle, Aspiration And Injection, Disposable), a Class I device regulated under 21 CFR 878.4800. Medical Device Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 8, 1998
Date Received
December 19, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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