The following data is part of a premarket notification filed by Prisma Systems with the FDA for Iron Qvet.
Device ID | K943029 |
510k Number | K943029 |
Device Name: | IRON QVET |
Classification | Photometric Method, Iron (non-heme) |
Applicant | PRISMA SYSTEMS 1721 BLACK RIVER BLVD. Rome, NY 13440 |
Contact | Larry Beasley |
Correspondent | Larry Beasley PRISMA SYSTEMS 1721 BLACK RIVER BLVD. Rome, NY 13440 |
Product Code | JIY |
CFR Regulation Number | 862.1410 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-06-27 |
Decision Date | 1994-12-02 |