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FDA 510(k)

IDAS INFUSION SET

K-Number: K830194 · 1983-03-29

Decision Date1983-03-29
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IDAS INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Idas America, Ltd.. It received FDA 510(k) clearance on 1983-03-29 under 510(k) number K830194. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IDAS INFUSION SET?

IDAS INFUSION SET is a medical device that received FDA 510(k) clearance on 1983-03-29. The listed applicant is Idas America, Ltd.. The 510(k) number is K830194.

When did IDAS INFUSION SET receive FDA 510(k) clearance?

IDAS INFUSION SET received FDA 510(k) clearance on 1983-03-29, under 510(k) number K830194.

Who is the listed applicant for IDAS INFUSION SET?

The FDA 510(k) record lists Idas America, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IDAS INFUSION SET?

The FDA product code for IDAS INFUSION SET is FPA.

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.

Related Devices (Code: FPA)

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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