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FDA 510(k)

3.0 ML RESERVOIR, MODEL 103/193

K-Number: K991936 · 2000-01-18

ApplicantMedtronic Minimed
Decision Date2000-01-18
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

3.0 ML RESERVOIR, MODEL 103/193 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Minimed. It received FDA 510(k) clearance on 2000-01-18 under 510(k) number K991936. 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 3.0 ML RESERVOIR, MODEL 103/193?

3.0 ML RESERVOIR, MODEL 103/193 is a medical device that received FDA 510(k) clearance on 2000-01-18. The listed applicant is Medtronic Minimed. The 510(k) number is K991936.

When did 3.0 ML RESERVOIR, MODEL 103/193 receive FDA 510(k) clearance?

3.0 ML RESERVOIR, MODEL 103/193 received FDA 510(k) clearance on 2000-01-18, under 510(k) number K991936.

Who is the listed applicant for 3.0 ML RESERVOIR, MODEL 103/193?

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 3.0 ML RESERVOIR, MODEL 103/193?

The FDA product code for 3.0 ML RESERVOIR, MODEL 103/193 is 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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