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FDA 510(k)

IVAC 260 SERIES VOLUME TRIC INFUSION CON

K-Number: K801861 · 1980-08-27

ApplicantY
Decision Date1980-08-27
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVAC 260 SERIES VOLUME TRIC INFUSION CON is the device name listed in this FDA 510(k) record. The listed applicant is Y. It received FDA 510(k) clearance on 1980-08-27 under 510(k) number K801861. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IVAC 260 SERIES VOLUME TRIC INFUSION CON?

IVAC 260 SERIES VOLUME TRIC INFUSION CON is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Y. The 510(k) number is K801861.

When did IVAC 260 SERIES VOLUME TRIC INFUSION CON receive FDA 510(k) clearance?

IVAC 260 SERIES VOLUME TRIC INFUSION CON received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801861.

Who is the listed applicant for IVAC 260 SERIES VOLUME TRIC INFUSION CON?

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 260 SERIES VOLUME TRIC INFUSION CON?

The FDA product code for IVAC 260 SERIES VOLUME TRIC INFUSION CON is LDR.

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Other records listing Y 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.

K955846MODEL 2082 TEMP PLUS III THERMOMETER/MODEL 2087 TEMP PLUS III WALL MOUNT THERMOMETERK960280IVAC NEEDLE FREE VALVE ADMINISTRATION SETSK953225IVAC BALL VALCE ADMIN. SETSK934095IVAC VENTED SYRINGE ADAPTER ADMINISTRATION SETSK940897IVAC NEEDLELESS INFECTION VALVE ADMINISTRATION SETK931550EZ ADMINISTRATION SET

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Related Devices (Code: LDR)

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.

K242693DEKA Infusion System, DEKA Administration SetDeka Research and Development CorporationK232316DEKA Infusion System, DEKA Administration SetDeka Research and DevelopmentK153760Volumetric Infusion ControllerDEKA Research & DevelopmentK963136PACER MODEL 100 INFUSION CONTROLLERHealth Watch, Inc.K971826ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500Alexander Mfg. Co.K971865ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3PAlexander Mfg. Co.

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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