The following data is part of a premarket notification filed by Stanbio Laboratory with the FDA for Rapet Crp.
Device ID | K974429 |
510k Number | K974429 |
Device Name: | RAPET CRP |
Classification | System, Test, C-reactive Protein |
Applicant | STANBIO LABORATORY 2930 EAST HOUSTON ST. San Antonio, TX 78202 |
Contact | Kirk Johnson |
Correspondent | Kirk Johnson STANBIO LABORATORY 2930 EAST HOUSTON ST. San Antonio, TX 78202 |
Product Code | DCN |
CFR Regulation Number | 866.5270 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-11-24 |
Decision Date | 1998-02-18 |
Summary: | summary |