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FDA 510(k)

I.V. TUBING ORGANIZER

K-Number: K790901 · 1979-06-27

Decision Date1979-06-27
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. TUBING ORGANIZER is the device name listed in this FDA 510(k) record. The listed applicant is Acumed Instruments Corp.. It received FDA 510(k) clearance on 1979-06-27 under 510(k) number K790901. 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 I.V. TUBING ORGANIZER?

I.V. TUBING ORGANIZER is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is Acumed Instruments Corp.. The 510(k) number is K790901.

When did I.V. TUBING ORGANIZER receive FDA 510(k) clearance?

I.V. TUBING ORGANIZER received FDA 510(k) clearance on 1979-06-27, under 510(k) number K790901.

Who is the listed applicant for I.V. TUBING ORGANIZER?

The FDA 510(k) record lists Acumed Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I.V. TUBING ORGANIZER?

The FDA product code for I.V. TUBING ORGANIZER 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 Acumed Instruments Corp. 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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