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Angiosystems, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1037577

Devices
14
Registrations
FDA
FDA recalls
0

Catalogue14

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Company details

FDA FEI number
1037577
Address
7 HOPKINS PL., DUCKTOWN, TN, 37326

Frequently asked questions

How many devices does ANGIOSYSTEMS, INC. have in the registry?

The registry currently lists 14 devices for ANGIOSYSTEMS, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list ANGIOSYSTEMS, INC.'s devices?

Among its 14 most recently registered devices, ANGIOSYSTEMS, INC. has devices listed in FDA 510(k) (14 devices).

What risk classes do ANGIOSYSTEMS, INC.'s devices fall under?

Among its 14 most recently registered devices, the classes recorded for ANGIOSYSTEMS, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from ANGIOSYSTEMS, INC. in the registry?

The most recently registered devices listed for ANGIOSYSTEMS, INC. include STERILE DISPOSABLE DRAPE/OPHTHALMIC SURGERY, ANGIOSYS FEMORAL ANGIOGRAPHY DRAPE, SURGICAL PROCEDURE TRAY/LAPAROSCOPY CHOLECYSTECTOM and ANGIO SYS BRACHIAL ANGIO DRAPE.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.