The following data is part of a premarket notification filed by Confirma, Inc. with the FDA for Access Breast Coil 4/sms.
Device ID | K060547 |
510k Number | K060547 |
Device Name: | ACCESS BREAST COIL 4/SMS |
Classification | Coil, Magnetic Resonance, Specialty |
Applicant | CONFIRMA, INC. 821 KIRKLAND AVE. Kirkland, WA 98033 -6318 |
Contact | Patricia A Milbank |
Correspondent | Patricia A Milbank CONFIRMA, INC. 821 KIRKLAND AVE. Kirkland, WA 98033 -6318 |
Product Code | MOS |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-03-01 |
Decision Date | 2006-03-29 |
Summary: | summary |