DURHAM; NON CORING WINGED ADMINISTRATION SET
K-Number: K931119 · 1993-11-03
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Device Summary
Frequently Asked Questions
What is the DURHAM; NON CORING WINGED ADMINISTRATION SET?
DURHAM; NON CORING WINGED ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1993-11-03. The listed applicant is Intl. Medical Consultants. The 510(k) number is K931119.
When did DURHAM; NON CORING WINGED ADMINISTRATION SET receive FDA 510(k) clearance?
DURHAM; NON CORING WINGED ADMINISTRATION SET received FDA 510(k) clearance on 1993-11-03, under 510(k) number K931119.
Who is the listed applicant for DURHAM; NON CORING WINGED ADMINISTRATION SET?
The FDA 510(k) record lists Intl. Medical Consultants as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DURHAM; NON CORING WINGED ADMINISTRATION SET?
The FDA product code for DURHAM; NON CORING WINGED 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 Intl. Medical Consultants 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.
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