The following data is part of a premarket notification filed by M.d.l. S.r.l. with the FDA for Semicut Semi-automatic Biopsy Needle, Themy Automatic Disposable Biopsy Device, Palium Automatic Reusable Biopsy Device, Easycut Semi-automatic Biopsy Needle, Mdl Biopsy And Coaxial Introducer Needles.
Device ID | K160316 |
510k Number | K160316 |
Device Name: | SemiCut Semi-automatic Biopsy Needle, Themy Automatic Disposable Biopsy Device, Palium Automatic Reusable Biopsy Device, EasyCut Semi-automatic Biopsy Needle, MDL Biopsy And Coaxial Introducer Needles |
Classification | Instrument, Biopsy |
Applicant | M.D.L. S.r.l. Via Tavani 1/a Delebio (so), IT 23014 |
Contact | Marcello Dell'oca |
Correspondent | Barbara K Barbeau Vantage Consulting International, Ltd. 888 E Belvidere Rd, Suite 212 Grayslake, IL 60030 |
Product Code | KNW |
CFR Regulation Number | 876.1075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-02-05 |
Decision Date | 2016-10-27 |
Summary: | summary |