Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

I.V.I.D. FLUID ADMINISTRATION SET MARKER

K-Number: K944619 · 1995-01-26

Decision Date1995-01-26
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V.I.D. FLUID ADMINISTRATION SET MARKER is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Bioresearch Assoc.. It received FDA 510(k) clearance on 1995-01-26 under 510(k) number K944619. 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.I.D. FLUID ADMINISTRATION SET MARKER?

I.V.I.D. FLUID ADMINISTRATION SET MARKER is a medical device that received FDA 510(k) clearance on 1995-01-26. The listed applicant is Advanced Bioresearch Assoc.. The 510(k) number is K944619.

When did I.V.I.D. FLUID ADMINISTRATION SET MARKER receive FDA 510(k) clearance?

I.V.I.D. FLUID ADMINISTRATION SET MARKER received FDA 510(k) clearance on 1995-01-26, under 510(k) number K944619.

Who is the listed applicant for I.V.I.D. FLUID ADMINISTRATION SET MARKER?

The FDA 510(k) record lists Advanced Bioresearch Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I.V.I.D. FLUID ADMINISTRATION SET MARKER?

The FDA product code for I.V.I.D. FLUID ADMINISTRATION SET MARKER 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 Advanced Bioresearch Assoc. 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑