Surgi-Aid Endoscopics, Inc.
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- Devices
- 1
What Surgi-Aid Endoscopics, Inc. makes
Surgi-Aid Endoscopics, Inc. manufactures flexible biopsy forceps, designed for endoscopic procedures to obtain tissue samples for diagnostic evaluation.
The company’s products are regulated as Class II medical devices in the US and are listed under FDA’s 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Flexible Biopsy Forcep Ref K871809
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgi-Aid Endoscopics, Inc. have in the registry?
The registry currently lists 1 device for Surgi-Aid Endoscopics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgi-Aid Endoscopics, Inc.'s devices?
Among its 1 most recently registered device, Surgi-Aid Endoscopics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Surgi-Aid Endoscopics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Surgi-Aid Endoscopics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgi-Aid Endoscopics, Inc. in the registry?
The most recently registered devices listed for Surgi-Aid Endoscopics, Inc. include FLEXIBLE BIOPSY FORCEP.