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FDA 510(k)

IVY COMMANDEER

K-Number: K840942 · 1984-03-30

ApplicantIvy Medical, Inc.
Decision Date1984-03-30
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVY COMMANDEER is the device name listed in this FDA 510(k) record. The listed applicant is Ivy Medical, Inc.. It received FDA 510(k) clearance on 1984-03-30 under 510(k) number K840942. 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 IVY COMMANDEER?

IVY COMMANDEER is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is Ivy Medical, Inc.. The 510(k) number is K840942.

When did IVY COMMANDEER receive FDA 510(k) clearance?

IVY COMMANDEER received FDA 510(k) clearance on 1984-03-30, under 510(k) number K840942.

Who is the listed applicant for IVY COMMANDEER?

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

What is the FDA product code for IVY COMMANDEER?

The FDA product code for IVY COMMANDEER is LDR.

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.

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Other records listing Ivy Medical, Inc. 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.

K882167IVY COMMANDER, MODEL 600K870820IVY COMMANDER (MODEL 500)

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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