Franklin Diagnostics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Franklin Diagnostics, Inc. makes
Franklin Diagnostics, Inc. makes the Franklin Collector and the ThyroChek One-Step Rapid TSH Assay.
These devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Franklin Collector(R) Ref K884612
510(k) 510(k)Thyrochek One-Step Rapid Tsh Assay Ref K960195
510(k) 510(k)
Frequently asked questions
How many devices does Franklin Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for Franklin Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Franklin Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, Franklin Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Franklin Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Franklin Diagnostics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Franklin Diagnostics, Inc. in the registry?
The most recently registered devices listed for Franklin Diagnostics, Inc. include FRANKLIN COLLECTOR(R) and THYROCHEK ONE-STEP RAPID TSH ASSAY.