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FDA 510(k)

AVIATOR INSULIN PUMP

K-Number: K071788 · 2008-01-11

ApplicantAbbott Diabetes Care, Inc.
Decision Date2008-01-11
Product CodeLZG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AVIATOR INSULIN PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Diabetes Care, Inc.. It received FDA 510(k) clearance on 2008-01-11 under 510(k) number K071788. The device is classified under product code LZG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVIATOR INSULIN PUMP?

AVIATOR INSULIN PUMP is a medical device that received FDA 510(k) clearance on 2008-01-11. The listed applicant is Abbott Diabetes Care, Inc.. The 510(k) number is K071788.

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

AVIATOR INSULIN PUMP received FDA 510(k) clearance on 2008-01-11, under 510(k) number K071788.

Who is the listed applicant for AVIATOR INSULIN PUMP?

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

What is the FDA product code for AVIATOR INSULIN PUMP?

The FDA product code for AVIATOR INSULIN PUMP is LZG.

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Related Devices (Code: LZG)

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K262153Pivot Insulin Delivery SystemModular Medical, Inc.K253534Pivot Insulin Delivery SystemModular MedicalK240158Modular Medical MODD1 Insulin Delivery SystemModular Medical, Inc.K241622Extended Reservoir; MiniMed ReservoirMedtronic MinimedK223372Omnipod GO Insulin Delivery DeviceInsulet CorporationK210714Extended ReservoirMedtronic Minimed, 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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