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FDA 510(k)

INTRAVASCULAR ADMINISTRATION SET

K-Number: K833030 · 1983-11-03

Decision Date1983-11-03
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRAVASCULAR ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Gish Biomedical, Inc.. It received FDA 510(k) clearance on 1983-11-03 under 510(k) number K833030. 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 INTRAVASCULAR ADMINISTRATION SET?

INTRAVASCULAR ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1983-11-03. The listed applicant is Gish Biomedical, Inc.. The 510(k) number is K833030.

When did INTRAVASCULAR ADMINISTRATION SET receive FDA 510(k) clearance?

INTRAVASCULAR ADMINISTRATION SET received FDA 510(k) clearance on 1983-11-03, under 510(k) number K833030.

Who is the listed applicant for INTRAVASCULAR ADMINISTRATION SET?

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

What is the FDA product code for INTRAVASCULAR ADMINISTRATION SET?

The FDA product code for INTRAVASCULAR ADMINISTRATION 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 Gish Biomedical, 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 75 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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