The following data is part of a premarket notification filed by Amersham Corp. with the FDA for Amerlex-m Follicle Stimulating Hormone(fsh)radioim.
Device ID | K851361 |
510k Number | K851361 |
Device Name: | AMERLEX-M FOLLICLE STIMULATING HORMONE(FSH)RADIOIM |
Classification | Radioimmunoassay, Follicle-stimulating Hormone |
Applicant | AMERSHAM CORP. 2636 SOUTH CLEARBROOK DR. Arlington Heights, IL 60005 |
Contact | Philip M Fantasia |
Correspondent | Philip M Fantasia AMERSHAM CORP. 2636 SOUTH CLEARBROOK DR. Arlington Heights, IL 60005 |
Product Code | CGJ |
CFR Regulation Number | 862.1300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-04-04 |
Decision Date | 1985-05-07 |