The following data is part of a premarket notification filed by Pacific Biotech, Inc. with the FDA for Beta Quik Stat.
Device ID | K852327 |
510k Number | K852327 |
Device Name: | BETA QUIK STAT |
Classification | Visual, Pregnancy Hcg, Prescription Use |
Applicant | PACIFIC BIOTECH, INC. 9050 CAMINO SANTA FE San Diego, CA 92121 |
Contact | Shung-ho Chang |
Correspondent | Shung-ho Chang 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 | 1985-05-30 |
Decision Date | 1985-08-20 |