The following data is part of a premarket notification filed by J. D. Assoc. with the FDA for Ferrofast.
Device ID | K863109 |
510k Number | K863109 |
Device Name: | FERROFAST |
Classification | Photometric Method, Iron (non-heme) |
Applicant | J. D. ASSOC. 163 MONTCLAIR AVE. Montclair, NJ 07042 |
Contact | Di Pietro |
Correspondent | Di Pietro J. D. ASSOC. 163 MONTCLAIR AVE. Montclair, NJ 07042 |
Product Code | JIY |
CFR Regulation Number | 862.1410 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-08-13 |
Decision Date | 1986-11-24 |