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Mission Pharmacal Company

Also registered as Mission Pharmacal Co.

United Statesfrom the FDA registration address FDA establishment FEI 3000204446

Devices
3
Registrations
FDA
FDA recalls
0

Catalogue3

Newest first, rows 1-3 of 3

  • Urocystin Ref K843382

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Vacuum Erection Device (Ved) Ref K901223

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Maxilube Ref K943010

    Active Regimes: 510(k) Registry: 510(k) Class:I

Company details

FDA FEI number
3000204446
Address
38505 IH-10 WEST, BOERNE, TX, 78006

Frequently asked questions

How many devices does MISSION PHARMACAL COMPANY have in the registry?

The registry currently lists 3 devices for MISSION PHARMACAL COMPANY. Devices recorded under merged duplicate company entries are counted once.

Which registries list MISSION PHARMACAL COMPANY's devices?

Among its 3 most recently registered devices, MISSION PHARMACAL COMPANY has devices listed in FDA 510(k) (3 devices).

What risk classes do MISSION PHARMACAL COMPANY's devices fall under?

Among its 3 most recently registered devices, the classes recorded for MISSION PHARMACAL COMPANY's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from MISSION PHARMACAL COMPANY in the registry?

The most recently registered devices listed for MISSION PHARMACAL COMPANY include UROCYSTIN, VACUUM ERECTION DEVICE (VED) and MAXILUBE.

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.