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FDA 510(k), K172410, Portex NRFit Epidural Needles, Portex NRFit Spinal Needles, Portex NRFit Loss of Resistance (L.O.R.) Syringes., Portex EpiFuse Catheter Connector, Portex Regional Anaesthesia Portfolio Filters
FDA 510(k), K172410, Portex NRFit Epidural Needles, Portex NRFit Spinal Needles, Portex NRFit Loss of Resistance (L.O.R.) Syringes., Portex EpiFuse Catheter Connector, Portex Regional Anaesthesia Portfolio Filters
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$49.00 USD
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$49.00 USD
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510(K) Number: K172410
Device Name: Portex NRFit Epidural Needles, Portex NRFit Spinal Needles, Portex NRFit Loss of Resistance (L.O.R.) Syringes., Portex EpiFuse Catheter Connector, Portex Regional Anaesthesia Portfolio Filters
Manufacturer: Michael R. Johnson
Device Classification Name: Needle, Conduction, Anesthetic (W/Wo Introducer)
Regulation Number: BSP
Classification Product Code: KXA
Date Received: 08/09/2017
Decision Date: 06/01/2018
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: Portex NRFit Epidural Needles, Portex NRFit Spinal Needles, Portex NRFit Loss of Resistance (L.O.R.) Syringes., Portex EpiFuse Catheter Connector, Portex Regional Anaesthesia Portfolio Filters
Manufacturer: Michael R. Johnson
Device Classification Name: Needle, Conduction, Anesthetic (W/Wo Introducer)
Regulation Number: BSP
Classification Product Code: KXA
Date Received: 08/09/2017
Decision Date: 06/01/2018
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
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