Medco Mfg.
United Statesfrom the FDA registration address FDA FEI 3001451796
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Medco Mfg. makes
Medco Mfg. manufactures the MEDCO ASPIRATOR IV, a device designed for suctioning fluids from intravenous lines or medical tubing in clinical settings.
The MEDCO ASPIRATOR IV is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Medco Aspirator Iv Ref K982371
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3001451796
- Address
- 8319 THORA No. A1, SPRING, TX, 77379
Frequently asked questions
How many devices does Medco Mfg. have in the registry?
The registry currently lists 1 device for Medco Mfg.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medco Mfg.'s devices?
Among its 1 most recently registered device, Medco Mfg. has devices listed in FDA 510(k) (1 device).
What risk classes do Medco Mfg.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medco Mfg.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medco Mfg. in the registry?
The most recently registered devices listed for Medco Mfg. include MEDCO ASPIRATOR IV.