The following data is part of a premarket notification filed by Amedic Usa with the FDA for Trt (acuson) Needle Guide Kit, Sterile.
Device ID | K892068 |
510k Number | K892068 |
Device Name: | TRT (ACUSON) NEEDLE GUIDE KIT, STERILE |
Classification | Biopsy Needle |
Applicant | AMEDIC USA OXENSTIERNSGATAN 31 115 27 STOCKHOLM Sweden, SE |
Contact | Anders Weilandt |
Correspondent | Anders Weilandt AMEDIC USA OXENSTIERNSGATAN 31 115 27 STOCKHOLM Sweden, SE |
Product Code | FCG |
CFR Regulation Number | 876.1075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-03-30 |
Decision Date | 1989-08-04 |