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FDA 510(k)

KIT,I.V. START

K-Number: K940035 · 1994-06-03

ApplicantMason-Keller Corp.
Decision Date1994-06-03
Product CodeLYZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

KIT,I.V. START is the device name listed in this FDA 510(k) record. The listed applicant is Mason-Keller Corp.. It received FDA 510(k) clearance on 1994-06-03 under 510(k) number K940035. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the KIT,I.V. START?

KIT,I.V. START is a medical device that received FDA 510(k) clearance on 1994-06-03. The listed applicant is Mason-Keller Corp.. The 510(k) number is K940035.

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

KIT,I.V. START received FDA 510(k) clearance on 1994-06-03, under 510(k) number K940035.

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

The FDA 510(k) record lists Mason-Keller Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIT,I.V. START?

The FDA product code for KIT,I.V. START is LYZ.

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Other records listing Mason-Keller Corp. 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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