510(k) K945160

PARACENTESIS NEEDLES/CANNULAS by Tri-Med Specialties, Inc. — Product Code LRO

K945160 is an FDA 510(k) premarket notification submitted by Tri-Med Specialties, Inc. for the device "PARACENTESIS NEEDLES/CANNULAS". The FDA issued a decision of Substantially Equivalent on November 14, 1994. The device falls under product code LRO (General Surgery Tray), a Class II device regulated under 21 CFR 878.4370. Tri-Med Specialties, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 14, 1994
Date Received
October 21, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
General Surgery Tray
Device Class
Class II
Regulation Number
878.4370
Review Panel
SU
Submission Type

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance