510(k) K902177

MANAN BONE BIOPSY NEEDLE by Manan Medical Products, Inc. — Product Code GDM

K902177 is an FDA 510(k) premarket notification submitted by Manan Medical Products, Inc. for the device "MANAN BONE BIOPSY NEEDLE". The FDA issued a decision of Substantially Equivalent on September 5, 1990. The device falls under product code GDM (Needle, Aspiration And Injection, Reusable), a Class I device regulated under 21 CFR 878.4800. Manan Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 5, 1990
Date Received
May 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