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. ADMINISTRATION SET CONNECTING DEVICE

K-Number: K901151 · 1990-07-02

Decision Date1990-07-02
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. ADMINISTRATION SET CONNECTING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Dmd, Div. of Casta Pacific Co.. It received FDA 510(k) clearance on 1990-07-02 under 510(k) number K901151. 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. ADMINISTRATION SET CONNECTING DEVICE?

I.V. ADMINISTRATION SET CONNECTING DEVICE is a medical device that received FDA 510(k) clearance on 1990-07-02. The listed applicant is Dmd, Div. of Casta Pacific Co.. The 510(k) number is K901151.

When did I.V. ADMINISTRATION SET CONNECTING DEVICE receive FDA 510(k) clearance?

I.V. ADMINISTRATION SET CONNECTING DEVICE received FDA 510(k) clearance on 1990-07-02, under 510(k) number K901151.

Who is the listed applicant for I.V. ADMINISTRATION SET CONNECTING DEVICE?

The FDA 510(k) record lists Dmd, Div. of Casta Pacific Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I.V. ADMINISTRATION SET CONNECTING DEVICE?

The FDA product code for I.V. ADMINISTRATION SET CONNECTING DEVICE 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.

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.

↑