The following data is part of a premarket notification filed by Sangui Biotech, Inc. with the FDA for Sangui Biotech, Inc. Calcitonin Elisa Kit.
Device ID | K982491 |
510k Number | K982491 |
Device Name: | SANGUI BIOTECH, INC. CALCITONIN ELISA KIT |
Classification | Radioimmunoassay, Calcitonin |
Applicant | SANGUI BIOTECH, INC. 1508 BROOKHOLLOW DR., #354 Santa Ana, CA 92705 |
Contact | John J Kiang |
Correspondent | John J Kiang SANGUI BIOTECH, INC. 1508 BROOKHOLLOW DR., #354 Santa Ana, CA 92705 |
Product Code | JKR |
CFR Regulation Number | 862.1140 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-07-17 |
Decision Date | 1998-09-03 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
B24221CALHUE010 | K982491 | 000 |
00840239036483 | K982491 | 000 |
00083059070248 | K982491 | 000 |
08305900070248 | K982491 | 000 |
04048474036480 | K982491 | 000 |