Meyer Equipment Company, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Meyer Equipment Company, Inc. makes
Meyer Equipment Company, Inc. manufactures the MEC-I-TRON MINI (Model M-2) and MEC-I-TRON (Model P-1), which appear to be electrosurgical devices designed for tissue cutting and coagulation in surgical procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Mec-I-Tron Mini, Model M-2 Ref K895289
Regimes: 510(k) Registry: 510(k)Mec-I-Tron, Model P-1 Ref K873190
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Meyer Equipment Company, Inc. have in the registry?
The registry currently lists 2 devices for Meyer Equipment Company, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Meyer Equipment Company, Inc.'s devices?
Among its 2 most recently registered devices, Meyer Equipment Company, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Meyer Equipment Company, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Meyer Equipment Company, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Meyer Equipment Company, Inc. in the registry?
The most recently registered devices listed for Meyer Equipment Company, Inc. include MEC-I-TRON MINI, MODEL M-2 and MEC-I-TRON, MODEL P-1.