Esco Precision, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Esco Precision, Inc. makes
Esco Precision, Inc. makes hot biopsy forceps and non-electric biopsy forceps.
The company's 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
Hot Biopsy Forceps Ref K905088
Regimes: 510(k) Registry: 510(k)Non-Electric Biopsy Forceps Ref K900015
Regimes: 510(k) Registry: 510(k)Non-Electric Biopsy Forceps Ref K900065
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Esco Precision, Inc. have in the registry?
The registry currently lists 3 devices for Esco Precision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Esco Precision, Inc.'s devices?
Among its 3 most recently registered devices, Esco Precision, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Esco Precision, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Esco Precision, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Esco Precision, Inc. in the registry?
The most recently registered devices listed for Esco Precision, Inc. include HOT BIOPSY FORCEPS and NON-ELECTRIC BIOPSY FORCEPS.