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FDA 510(k)

PSI-TEC PERISTALTIC INFILTRATION PUMP

K-Number: K040149 · 2004-06-03

ApplicantByron Medical
Decision Date2004-06-03
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PSI-TEC PERISTALTIC INFILTRATION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Byron Medical. It received FDA 510(k) clearance on 2004-06-03 under 510(k) number K040149. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PSI-TEC PERISTALTIC INFILTRATION PUMP?

PSI-TEC PERISTALTIC INFILTRATION PUMP is a medical device that received FDA 510(k) clearance on 2004-06-03. The listed applicant is Byron Medical. The 510(k) number is K040149.

When did PSI-TEC PERISTALTIC INFILTRATION PUMP receive FDA 510(k) clearance?

PSI-TEC PERISTALTIC INFILTRATION PUMP received FDA 510(k) clearance on 2004-06-03, under 510(k) number K040149.

Who is the listed applicant for PSI-TEC PERISTALTIC INFILTRATION PUMP?

The FDA 510(k) record lists Byron Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PSI-TEC PERISTALTIC INFILTRATION PUMP?

The FDA product code for PSI-TEC PERISTALTIC INFILTRATION PUMP is FRN.

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Other records listing Byron Medical as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K001803ACCELERATOR RECIPROCATING CANNULAK981215PSI-TEC LIPOSUCTION ASPIRATORK981172LIPOPLASTY/ LIPOSUCTION ASPIRATION AND TUMESCENT INFUSION CANNULAE AND NEEDLESK980738PSI-TEC SYRINGE INFUSION PUMP AND ACCESSORIES FOR GENERAL FLUID IRRIGAION/INFILTRATIONK980392PSI-TEC ASPIRATORK974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING

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Related Devices (Code: FRN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253703RemunityPRO+ Pump for Remodulin® (treprostinil) InjectionDeka R&D CorpK252015FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate TubingKoru Medical Systems, Inc.K251636Spectrum IQ Infusion System with Dose IQ Safety Software (3570009)Baxter Healthcare CorporationK251640SIGMA Spectrum Infusion Pump with Master Drug LibraryBaxter Healthcare CorporationK242752MRidium 3870 MRI Infusion Pump System (3870)Iradimed CorporationK243855BD Alaris Infusion System with Guardrails Suite MXCarefusion 303, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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