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FDA 510(k)

IV SET WITH GRADUATED CHAMBER

K-Number: K781744 · 1978-12-07

Decision Date1978-12-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV SET WITH GRADUATED CHAMBER is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1978-12-07 under 510(k) number K781744. 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 IV SET WITH GRADUATED CHAMBER?

IV SET WITH GRADUATED CHAMBER is a medical device that received FDA 510(k) clearance on 1978-12-07. The listed applicant is National Patent Development Corp.. The 510(k) number is K781744.

When did IV SET WITH GRADUATED CHAMBER receive FDA 510(k) clearance?

IV SET WITH GRADUATED CHAMBER received FDA 510(k) clearance on 1978-12-07, under 510(k) number K781744.

Who is the listed applicant for IV SET WITH GRADUATED CHAMBER?

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

What is the FDA product code for IV SET WITH GRADUATED CHAMBER?

The FDA product code for IV SET WITH GRADUATED CHAMBER 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 National Patent Development 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 34 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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