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FDA 510(k)

MODIFIED MINIMED III INFUSION PUMP

K-Number: K895436 · 1990-05-24

ApplicantMedtronic Minimed
Decision Date1990-05-24
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFIED MINIMED III INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Minimed. It received FDA 510(k) clearance on 1990-05-24 under 510(k) number K895436. 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 MODIFIED MINIMED III INFUSION PUMP?

MODIFIED MINIMED III INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1990-05-24. The listed applicant is Medtronic Minimed. The 510(k) number is K895436.

When did MODIFIED MINIMED III INFUSION PUMP receive FDA 510(k) clearance?

MODIFIED MINIMED III INFUSION PUMP received FDA 510(k) clearance on 1990-05-24, under 510(k) number K895436.

Who is the listed applicant for MODIFIED MINIMED III INFUSION PUMP?

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

What is the FDA product code for MODIFIED MINIMED III INFUSION PUMP?

The FDA product code for MODIFIED MINIMED III INFUSION PUMP is FRN.

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Other records listing Medtronic Minimed as applicant

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Related Devices (Code: FRN)

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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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