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FDA 510(k)

MODEL 304-S EXTERNAL MICRO-VOLUME INFUSION PUMP

K-Number: K864327 · 1987-02-06

ApplicantMedtronic Minimed
Decision Date1987-02-06
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 304-S EXTERNAL MICRO-VOLUME 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 1987-02-06 under 510(k) number K864327. The device is classified under product code FRW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 304-S EXTERNAL MICRO-VOLUME INFUSION PUMP?

MODEL 304-S EXTERNAL MICRO-VOLUME INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1987-02-06. The listed applicant is Medtronic Minimed. The 510(k) number is K864327.

When did MODEL 304-S EXTERNAL MICRO-VOLUME INFUSION PUMP receive FDA 510(k) clearance?

MODEL 304-S EXTERNAL MICRO-VOLUME INFUSION PUMP received FDA 510(k) clearance on 1987-02-06, under 510(k) number K864327.

Who is the listed applicant for MODEL 304-S EXTERNAL MICRO-VOLUME 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 MODEL 304-S EXTERNAL MICRO-VOLUME INFUSION PUMP?

The FDA product code for MODEL 304-S EXTERNAL MICRO-VOLUME INFUSION PUMP is FRW.

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Related Devices (Code: FRW)

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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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