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FDA 510(k)

INTRAVENOUS INFUSION CONTROLLER

K-Number: K834106 · 1984-05-30

ApplicantCutter Laboratories, Inc.
Decision Date1984-05-30
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRAVENOUS INFUSION CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1984-05-30 under 510(k) number K834106. 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 INTRAVENOUS INFUSION CONTROLLER?

INTRAVENOUS INFUSION CONTROLLER is a medical device that received FDA 510(k) clearance on 1984-05-30. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K834106.

When did INTRAVENOUS INFUSION CONTROLLER receive FDA 510(k) clearance?

INTRAVENOUS INFUSION CONTROLLER received FDA 510(k) clearance on 1984-05-30, under 510(k) number K834106.

Who is the listed applicant for INTRAVENOUS INFUSION CONTROLLER?

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

What is the FDA product code for INTRAVENOUS INFUSION CONTROLLER?

The FDA product code for INTRAVENOUS INFUSION CONTROLLER is LDR.

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Other records listing Cutter Laboratories, 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.

K861315HYPERBARIC PENETRATION EXTENSION SETK854106BAYSILEXK842324PERFOURMK832237ORTHOPEDIC CASTING TAPE MAXCASTK823214DOSIMETRIC RELEASE PROGRAM - ADMIN. SETK821326CUTTER BOND POLYCARBOXYLATE CEMENT

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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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