Medical Device Manufacturer · IT , Due Carrare Padova

Artiglass Srl

2 submissions · 2 cleared · Since 2013
2
Total
2
Cleared
0
Denied

Artiglass Srl — FDA 510(k) Submissions

Artiglass Srl has submitted 2 FDA 510(k) premarket notifications since 2013, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Piston Syringe With Neuraxial Connector ? Epidural, Peripheral, And/or Indirect Cerebral Spinal Fluid Contact, Syringe, Piston . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Anesthesiology 1 General Hospital 1