The following data is part of a premarket notification filed by Techno-path Manufacturing Ltd. with the FDA for Multichem P.
Device ID | K131992 |
510k Number | K131992 |
Device Name: | MULTICHEM P |
Classification | Multi-analyte Controls, All Kinds (assayed) |
Applicant | TECHNO-PATH MANUFACTURING LTD. 325 BIG ELM ST. Highland Village, TX 75077 |
Contact | Stephanie G Garth |
Correspondent | Stephanie G Garth TECHNO-PATH MANUFACTURING LTD. 325 BIG ELM ST. Highland Village, TX 75077 |
Product Code | JJY |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-06-28 |
Decision Date | 2013-09-25 |
Summary: | summary |