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FDA 510(k)

IV START KIT

K-Number: K924538 · 1993-07-02

ApplicantCml, Inc.
Decision Date1993-07-02
Product CodeLRS
Advisory CommitteeHO
DecisionUnknown

Device Summary

IV START KIT is the device name listed in this FDA 510(k) record. The listed applicant is Cml, Inc.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K924538. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the IV START KIT?

IV START KIT is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Cml, Inc.. The 510(k) number is K924538.

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

IV START KIT received FDA 510(k) clearance on 1993-07-02, under 510(k) number K924538.

Who is the listed applicant for IV START KIT?

The FDA 510(k) record lists Cml, 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 Cml, 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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