The following data is part of a premarket notification filed by Meadox Surgimed, Inc. with the FDA for Meadox Surgimed Breast Localization Wire Set/only.
Device ID | K854262 |
510k Number | K854262 |
Device Name: | MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY |
Classification | Guide, Surgical, Instrument |
Applicant | MEADOX SURGIMED, INC. 112 BAUER DR. Oakland, NJ 07436 |
Contact | Scott Mindrebo |
Correspondent | Scott Mindrebo MEADOX SURGIMED, INC. 112 BAUER DR. Oakland, NJ 07436 |
Product Code | FZX |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-10-23 |
Decision Date | 1985-12-24 |