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FDA 510(k)

IVAC(R) SITE-SAVER(R) VOLUMETRIC CONTROLLER - 280+

K-Number: K874491 · 1988-02-25

ApplicantY
Decision Date1988-02-25
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVAC(R) SITE-SAVER(R) VOLUMETRIC CONTROLLER - 280+ is the device name listed in this FDA 510(k) record. The listed applicant is Y. It received FDA 510(k) clearance on 1988-02-25 under 510(k) number K874491. 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(R) SITE-SAVER(R) VOLUMETRIC CONTROLLER - 280+?

IVAC(R) SITE-SAVER(R) VOLUMETRIC CONTROLLER - 280+ is a medical device that received FDA 510(k) clearance on 1988-02-25. The listed applicant is Y. The 510(k) number is K874491.

When did IVAC(R) SITE-SAVER(R) VOLUMETRIC CONTROLLER - 280+ receive FDA 510(k) clearance?

IVAC(R) SITE-SAVER(R) VOLUMETRIC CONTROLLER - 280+ received FDA 510(k) clearance on 1988-02-25, under 510(k) number K874491.

Who is the listed applicant for IVAC(R) SITE-SAVER(R) VOLUMETRIC CONTROLLER - 280+?

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) SITE-SAVER(R) VOLUMETRIC CONTROLLER - 280+?

The FDA product code for IVAC(R) SITE-SAVER(R) VOLUMETRIC CONTROLLER - 280+ 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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