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FDA 510(k)

AMBULATORY INSULIN INFUSION PUMP

K-Number: K832923 · 1983-11-03

ApplicantCaridac Pacemakers, Inc.
Decision Date1983-11-03
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AMBULATORY INSULIN INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Caridac Pacemakers, Inc.. It received FDA 510(k) clearance on 1983-11-03 under 510(k) number K832923. 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 AMBULATORY INSULIN INFUSION PUMP?

AMBULATORY INSULIN INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1983-11-03. The listed applicant is Caridac Pacemakers, Inc.. The 510(k) number is K832923.

When did AMBULATORY INSULIN INFUSION PUMP receive FDA 510(k) clearance?

AMBULATORY INSULIN INFUSION PUMP received FDA 510(k) clearance on 1983-11-03, under 510(k) number K832923.

Who is the listed applicant for AMBULATORY INSULIN INFUSION PUMP?

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

What is the FDA product code for AMBULATORY INSULIN INFUSION PUMP?

The FDA product code for AMBULATORY INSULIN INFUSION PUMP is FRN.

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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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