The following data is part of a premarket notification filed by Pacific Biotech, Inc. with the FDA for Modified Beta Quik Stat Eia Kit.
| Device ID | K882895 |
| 510k Number | K882895 |
| Device Name: | MODIFIED BETA QUIK STAT EIA KIT |
| Classification | System, Test, Human Chorionic Gonadotropin |
| Applicant | PACIFIC BIOTECH, INC. 9050 CAMINO SANTA FE San Diego, CA 92121 |
| Contact | Shu-ching Cheng |
| Correspondent | Shu-ching Cheng PACIFIC BIOTECH, INC. 9050 CAMINO SANTA FE San Diego, CA 92121 |
| Product Code | DHA |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-07-11 |
| Decision Date | 1988-10-12 |