The following data is part of a premarket notification filed by Biogenex Laboratories with the FDA for Pregnagen(tm).
Device ID | K882002 |
510k Number | K882002 |
Device Name: | PREGNAGEN(TM) |
Classification | Visual, Pregnancy Hcg, Prescription Use |
Applicant | BIOGENEX LABORATORIES 4600 NORRIS CANYON RD. San Ramon, CA 94583 |
Contact | Krishan L Kalra,phd |
Correspondent | Krishan L Kalra,phd BIOGENEX LABORATORIES 4600 NORRIS CANYON RD. San Ramon, CA 94583 |
Product Code | JHI |
CFR Regulation Number | 862.1155 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-05-13 |
Decision Date | 1988-09-09 |