The following data is part of a premarket notification filed by Biopsybell S.r.l. with the FDA for Manual-bone-marrow-biopsy-needles, Semi-automatic-biopsy-needles, Automatic-biopsy-needles.
Device ID | K130616 |
510k Number | K130616 |
Device Name: | MANUAL-BONE-MARROW-BIOPSY-NEEDLES, SEMI-AUTOMATIC-BIOPSY-NEEDLES, AUTOMATIC-BIOPSY-NEEDLES |
Classification | Instrument, Biopsy |
Applicant | BIOPSYBELL S.R.L. 62 GERDES AVE. Verona, NJ 07004 |
Contact | Willer Ghelfi |
Correspondent | Willer Ghelfi BIOPSYBELL S.R.L. 62 GERDES AVE. Verona, NJ 07004 |
Product Code | KNW |
CFR Regulation Number | 876.1075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-03-07 |
Decision Date | 2014-02-07 |
Summary: | summary |