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FDA 510(k)

PARADIGMPAL, MODEL MMT-7330

K-Number: K031541 · 2003-11-18

ApplicantMinimed, Inc.
Decision Date2003-11-18
Product CodeLZG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PARADIGMPAL, MODEL MMT-7330 is the device name listed in this FDA 510(k) record. The listed applicant is Minimed, Inc.. It received FDA 510(k) clearance on 2003-11-18 under 510(k) number K031541. 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 PARADIGMPAL, MODEL MMT-7330?

PARADIGMPAL, MODEL MMT-7330 is a medical device that received FDA 510(k) clearance on 2003-11-18. The listed applicant is Minimed, Inc.. The 510(k) number is K031541.

When did PARADIGMPAL, MODEL MMT-7330 receive FDA 510(k) clearance?

PARADIGMPAL, MODEL MMT-7330 received FDA 510(k) clearance on 2003-11-18, under 510(k) number K031541.

Who is the listed applicant for PARADIGMPAL, MODEL MMT-7330?

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

What is the FDA product code for PARADIGMPAL, MODEL MMT-7330?

The FDA product code for PARADIGMPAL, MODEL MMT-7330 is LZG.

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Other records listing Minimed, 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.

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Related Devices (Code: LZG)

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.

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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