The following data is part of a premarket notification filed by Volpara Health Technologies Limited with the FDA for Volpara Imaging Software.
Device ID | K182310 |
510k Number | K182310 |
Device Name: | Volpara Imaging Software |
Classification | System, Image Processing, Radiological |
Applicant | Volpara Health Technologies Limited Level 7, 44 Victoria Street, Wellington Central Wellington, NZ 6011 |
Contact | Ralph Highnam |
Correspondent | Ralph Highnam Volpara Health Technologies Limited Level 7, 44 Victoria Street, Wellington Central Wellington, NZ 6011 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-08-24 |
Decision Date | 2018-09-21 |
Summary: | summary |