510(k) K914941

SIMON BREAST LESION LOCALIZATION NEEDLE by Manan Medical Products, Inc. — Product Code GDF

K914941 is an FDA 510(k) premarket notification submitted by Manan Medical Products, Inc. for the device "SIMON BREAST LESION LOCALIZATION NEEDLE". The FDA issued a decision of Substantially Equivalent on May 14, 1992. The device falls under product code GDF (Guide, Needle, Surgical), 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
May 14, 1992
Date Received
November 4, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Guide, Needle, Surgical
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type