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FDA 510(k)

MODEL 504-S EXTERNAL INFUSION PUMP FOR DIABETICS

K-Number: K864517 · 1986-12-12

Decision Date1986-12-12
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 504-S EXTERNAL INFUSION PUMP FOR DIABETICS is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Minimed. It received FDA 510(k) clearance on 1986-12-12 under 510(k) number K864517. 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 MODEL 504-S EXTERNAL INFUSION PUMP FOR DIABETICS?

MODEL 504-S EXTERNAL INFUSION PUMP FOR DIABETICS is a medical device that received FDA 510(k) clearance on 1986-12-12. The listed applicant is Medtronic Minimed. The 510(k) number is K864517.

When did MODEL 504-S EXTERNAL INFUSION PUMP FOR DIABETICS receive FDA 510(k) clearance?

MODEL 504-S EXTERNAL INFUSION PUMP FOR DIABETICS received FDA 510(k) clearance on 1986-12-12, under 510(k) number K864517.

Who is the listed applicant for MODEL 504-S EXTERNAL INFUSION PUMP FOR DIABETICS?

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 504-S EXTERNAL INFUSION PUMP FOR DIABETICS?

The FDA product code for MODEL 504-S EXTERNAL INFUSION PUMP FOR DIABETICS is FRN.

Related Clinical Trials

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.

Other records listing Medtronic Minimed 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.

View all 49 devices →

Related Devices (Code: FRN)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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