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FDA 510(k)

DISPOSABLE INTRAVENOUS INJECTION SYSTEM

K-Number: K821764 · 1982-06-29

Decision Date1982-06-29
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE INTRAVENOUS INJECTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Systems Research. It received FDA 510(k) clearance on 1982-06-29 under 510(k) number K821764. 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 DISPOSABLE INTRAVENOUS INJECTION SYSTEM?

DISPOSABLE INTRAVENOUS INJECTION SYSTEM is a medical device that received FDA 510(k) clearance on 1982-06-29. The listed applicant is Medical Systems Research. The 510(k) number is K821764.

When did DISPOSABLE INTRAVENOUS INJECTION SYSTEM receive FDA 510(k) clearance?

DISPOSABLE INTRAVENOUS INJECTION SYSTEM received FDA 510(k) clearance on 1982-06-29, under 510(k) number K821764.

Who is the listed applicant for DISPOSABLE INTRAVENOUS INJECTION SYSTEM?

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

What is the FDA product code for DISPOSABLE INTRAVENOUS INJECTION SYSTEM?

The FDA product code for DISPOSABLE INTRAVENOUS INJECTION SYSTEM 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 Medical Systems Research 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.

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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