Shamrock Manufacturing Company
Country not established
- Devices
- 2
What Shamrock Manufacturing Company makes
Shamrock Manufacturing Company produces powder-free nitrile neoprene examination gloves, including a standard line and sizes ranging from small to extra-large.
These products are classified as Class I medical devices and are listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Powder Free Synthetic Nitrile Neoprene Examination Gloves, Sizes Small, Medium, Large, And X-Large Ref K030386
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Shamrock Manufacturing Company have in the registry?
The registry currently lists 2 devices for Shamrock Manufacturing Company. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shamrock Manufacturing Company's devices?
Among its 2 most recently registered devices, Shamrock Manufacturing Company has devices listed in FDA 510(k) (2 devices).
What risk classes do Shamrock Manufacturing Company's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Shamrock Manufacturing Company's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Shamrock Manufacturing Company in the registry?
The most recently registered devices listed for Shamrock Manufacturing Company include POWDERFREE NITRILE NEOPRENE EXAMINATION GLOVES (PULPLE) and POWDER FREE SYNTHETIC NITRILE NEOPRENE EXAMINATION GLOVES, SIZES SMALL, MEDIUM, LARGE, AND X-LARGE.