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FDA 510(k)

IV START KIT

K-Number: K871281 · 1987-05-27

Decision Date1987-05-27
Product CodeLRS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV START KIT is the device name listed in this FDA 510(k) record. The listed applicant is The Jarid Group, Inc.. It received FDA 510(k) clearance on 1987-05-27 under 510(k) number K871281. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IV START KIT?

IV START KIT is a medical device that received FDA 510(k) clearance on 1987-05-27. The listed applicant is The Jarid Group, Inc.. The 510(k) number is K871281.

When did IV START KIT receive FDA 510(k) clearance?

IV START KIT received FDA 510(k) clearance on 1987-05-27, under 510(k) number K871281.

Who is the listed applicant for IV START KIT?

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

What is the FDA product code for IV START KIT?

The FDA product code for IV START KIT is LRS.

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 The Jarid Group, 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: LRS)

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

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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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