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FDA 510(k)

KIT PAK I.V. START KIT

K-Number: K924051 · 1993-06-22

ApplicantKit Pak, Inc.
Decision Date1993-06-22
Product CodeLYY
Advisory CommitteeHO
DecisionUnknown

Device Summary

KIT PAK I.V. START KIT is the device name listed in this FDA 510(k) record. The listed applicant is Kit Pak, Inc.. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K924051. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the KIT PAK I.V. START KIT?

KIT PAK I.V. START KIT is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Kit Pak, Inc.. The 510(k) number is K924051.

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

KIT PAK I.V. START KIT received FDA 510(k) clearance on 1993-06-22, under 510(k) number K924051.

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

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

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

The FDA product code for KIT PAK I.V. START KIT is LYY.

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Other records listing Kit Pak, 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.

K942959KIT PAK WET SALINE DRESSINGK941499KIT PAK DRESSING CHANGE TRAYK932310KIT PAK INCONTINENT SKIN CARE KITK934080URINARY DRAINAGE BAGK931013FOLEY CATHETER TRAYK923905WOUND DRESSING KIT

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Related Devices (Code: LYY)

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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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