The following data is part of a premarket notification filed by Vanguard Biomedical Corp. with the FDA for Modified Homeclinic Pregnancy Test.
| Device ID | K895560 |
| 510k Number | K895560 |
| Device Name: | MODIFIED HOMECLINIC PREGNANCY TEST |
| Classification | Kit, Test, Pregnancy, Hcg, Over The Counter |
| Applicant | VANGUARD BIOMEDICAL CORP. 7822 CONVOY COURT San Diego, CA 92111 |
| Contact | Chiu, Ph.d. |
| Correspondent | Chiu, Ph.d. VANGUARD BIOMEDICAL CORP. 7822 CONVOY COURT San Diego, CA 92111 |
| Product Code | LCX |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-09-06 |
| Decision Date | 1989-11-13 |