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FDA 510(k)

IDEAS' PORT

K-Number: K913602 · 1992-01-02

Decision Date1992-01-02
Product CodeFMF
Advisory CommitteeHO
DecisionUnknown

Device Summary

IDEAS' PORT is the device name listed in this FDA 510(k) record. The listed applicant is Ideal Medical, Inc.. It received FDA 510(k) clearance on 1992-01-02 under 510(k) number K913602. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the IDEAS' PORT?

IDEAS' PORT is a medical device that received FDA 510(k) clearance on 1992-01-02. The listed applicant is Ideal Medical, Inc.. The 510(k) number is K913602.

When did IDEAS' PORT receive FDA 510(k) clearance?

IDEAS' PORT received FDA 510(k) clearance on 1992-01-02, under 510(k) number K913602.

Who is the listed applicant for IDEAS' PORT?

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

What is the FDA product code for IDEAS' PORT?

The FDA product code for IDEAS' PORT is FMF.

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 Ideal Medical, 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.

View all 16 devices →

Related Devices (Code: FMF)

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

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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