The following data is part of a premarket notification filed by Hygeia Sciences with the FDA for Hygeia Urine Pregnancy Test.
Device ID | K882192 |
510k Number | K882192 |
Device Name: | HYGEIA URINE PREGNANCY TEST |
Classification | System, Test, Human Chorionic Gonadotropin |
Applicant | HYGEIA SCIENCES 330 NEVADA ST. Newton, MA 02160 |
Contact | Cannon, Phd |
Correspondent | Cannon, Phd HYGEIA SCIENCES 330 NEVADA ST. Newton, MA 02160 |
Product Code | DHA |
CFR Regulation Number | 862.1155 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-05-25 |
Decision Date | 1988-11-10 |