Pipeline Medical Products, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3041679947
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
AeroJet Ventilation Catheter Ref K243579
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3041679947
- Address
- 122 Park Ave, Weymouth, MA, 02190
Frequently asked questions
How many devices does PIPELINE MEDICAL PRODUCTS, LLC have in the registry?
The registry currently lists 1 device for PIPELINE MEDICAL PRODUCTS, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list PIPELINE MEDICAL PRODUCTS, LLC's devices?
Among its 1 most recently registered device, PIPELINE MEDICAL PRODUCTS, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do PIPELINE MEDICAL PRODUCTS, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for PIPELINE MEDICAL PRODUCTS, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PIPELINE MEDICAL PRODUCTS, LLC in the registry?
The most recently registered devices listed for PIPELINE MEDICAL PRODUCTS, LLC include AeroJet Ventilation Catheter.