Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AVI INFUSION PUMPS, ADDITIONAL INTENDED USE

K-Number: K933006 · 1993-10-25

Applicant3M Health Care, Ltd.
Decision Date1993-10-25
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AVI INFUSION PUMPS, ADDITIONAL INTENDED USE is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Ltd.. It received FDA 510(k) clearance on 1993-10-25 under 510(k) number K933006. 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 AVI INFUSION PUMPS, ADDITIONAL INTENDED USE?

AVI INFUSION PUMPS, ADDITIONAL INTENDED USE is a medical device that received FDA 510(k) clearance on 1993-10-25. The listed applicant is 3M Health Care, Ltd.. The 510(k) number is K933006.

When did AVI INFUSION PUMPS, ADDITIONAL INTENDED USE receive FDA 510(k) clearance?

AVI INFUSION PUMPS, ADDITIONAL INTENDED USE received FDA 510(k) clearance on 1993-10-25, under 510(k) number K933006.

Who is the listed applicant for AVI INFUSION PUMPS, ADDITIONAL INTENDED USE?

The FDA 510(k) record lists 3M Health Care, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVI INFUSION PUMPS, ADDITIONAL INTENDED USE?

The FDA product code for AVI INFUSION PUMPS, ADDITIONAL INTENDED USE is FRN.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing 3M Health Care, Ltd. 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.

K953904SARNS 9000 UNIVERSAL ROLLER PUMPK926364ATTEST BRAND RAPID READOUT BIOLOGICAL IND. #129XK941534MODULAR VS-22 CEMENTED FEMORAL HIP SYSTEMK941748STERI-VAC GAS STERILIZER MODEL 8XLK9306813M PREVENTION FABRIC SURGICAL GOWN #78XXK9323073M MAXI-DRIVER II DBATTERY POWERED SYSTEM

View all 49 devices →

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.

↑