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FDA 510(k)

I.V. START KIT

K-Number: K863284 · 1986-09-22

Decision Date1986-09-22
Product Code
DecisionUnknown

Device Summary

I.V. START KIT is the device name listed in this FDA 510(k) record. The listed applicant is Welmed Systems, Inc.. It received FDA 510(k) clearance on 1986-09-22 under 510(k) number K863284. FDA Decision: Unknown.

Frequently Asked Questions

What is the I.V. START KIT?

I.V. START KIT is a medical device that received FDA 510(k) clearance on 1986-09-22. The listed applicant is Welmed Systems, Inc.. The 510(k) number is K863284.

When did I.V. START KIT receive FDA 510(k) clearance?

I.V. START KIT received FDA 510(k) clearance on 1986-09-22, under 510(k) number K863284.

Who is the listed applicant for I.V. START KIT?

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

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 Welmed Systems, 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.

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Official Source

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

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