The following data is part of a premarket notification filed by Pantex, Div. Bio-analysis, Inc. with the FDA for Prolactin Irma Immunomag.
Device ID | K914107 |
510k Number | K914107 |
Device Name: | PROLACTIN IRMA IMMUNOMAG |
Classification | Radioimmunoassay, Prolactin (lactogen) |
Applicant | PANTEX, DIV. BIO-ANALYSIS, INC. 1737 21ST ST. Santa Monica, CA 90404 |
Contact | Neil Y Chiamori |
Correspondent | Neil Y Chiamori PANTEX, DIV. BIO-ANALYSIS, INC. 1737 21ST ST. Santa Monica, CA 90404 |
Product Code | CFT |
CFR Regulation Number | 862.1625 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-09-13 |
Decision Date | 1991-09-30 |