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FDA 510(k)

ADMINISTRATIVE IV SET

K-Number: K832105 · 1983-09-12

Decision Date1983-09-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ADMINISTRATIVE IV SET is the device name listed in this FDA 510(k) record. The listed applicant is Lee Medical Intl., Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832105. 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 ADMINISTRATIVE IV SET?

ADMINISTRATIVE IV SET is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Lee Medical Intl., Inc.. The 510(k) number is K832105.

When did ADMINISTRATIVE IV SET receive FDA 510(k) clearance?

ADMINISTRATIVE IV SET received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832105.

Who is the listed applicant for ADMINISTRATIVE IV SET?

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

What is the FDA product code for ADMINISTRATIVE IV SET?

The FDA product code for ADMINISTRATIVE IV 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.

Other records listing Lee Medical Intl., 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 8 devices →

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

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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