The following data is part of a premarket notification filed by Pacific Biotech, Inc. with the FDA for Modified Hcg Irma Kit.
| Device ID | K883639 |
| 510k Number | K883639 |
| Device Name: | MODIFIED HCG IRMA KIT |
| Classification | Visual, Pregnancy Hcg, Prescription Use |
| 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 | JHI |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-08-25 |
| Decision Date | 1988-10-06 |