E & M Engineering, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 6
Catalogue
Electrosurgical Pencil Ref K936304
510(k) 510(k)Disposable Electrosurgery Grounding Pad Ref K984276
510(k) 510(k)Electrosurgical Unit Ref K921271
510(k) 510(k)Loop/Square Electrode Ref K952030
510(k) 510(k)Blade Electrode Ref K945531
510(k) 510(k)Reusable, Hand Controlled Esp Ref K936075
510(k) 510(k)
Frequently asked questions
How many devices does E & M Engineering, Inc. have in the registry?
The registry currently lists 6 devices for E & M Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list E & M Engineering, Inc.'s devices?
Among its 6 most recently registered devices, E & M Engineering, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do E & M Engineering, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for E & M Engineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from E & M Engineering, Inc. in the registry?
The most recently registered devices listed for E & M Engineering, Inc. include ELECTROSURGICAL PENCIL, DISPOSABLE ELECTROSURGERY GROUNDING PAD, ELECTROSURGICAL UNIT and LOOP/SQUARE ELECTRODE.