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FDA 510(k)

IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580+

K-Number: K873776 · 1987-12-03

ApplicantY
Decision Date1987-12-03
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580+ is the device name listed in this FDA 510(k) record. The listed applicant is Y. It received FDA 510(k) clearance on 1987-12-03 under 510(k) number K873776. 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 IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580+?

IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580+ is a medical device that received FDA 510(k) clearance on 1987-12-03. The listed applicant is Y. The 510(k) number is K873776.

When did IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580+ receive FDA 510(k) clearance?

IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580+ received FDA 510(k) clearance on 1987-12-03, under 510(k) number K873776.

Who is the listed applicant for IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580+?

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

What is the FDA product code for IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580+?

The FDA product code for IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580+ is FRN.

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Other records listing Y as applicant

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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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