I.V. START SET
K-Number: K791885 · 1979-10-22
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Device Summary
Frequently Asked Questions
What is the I.V. START SET?
I.V. START SET is a medical device that received FDA 510(k) clearance on 1979-10-22. The listed applicant is Ascep, Inc.. The 510(k) number is K791885.
When did I.V. START SET receive FDA 510(k) clearance?
I.V. START SET received FDA 510(k) clearance on 1979-10-22, under 510(k) number K791885.
Who is the listed applicant for I.V. START SET?
The FDA 510(k) record lists Ascep, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for I.V. START SET?
The FDA product code for I.V. START SET is KGX.
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 Ascep, 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.
Related Devices (Code: KGX)
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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