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FDA 510(k)

FAMILY FIRST AID KIT

K-Number: K935131 · 1994-03-23

Decision Date1994-03-23
Product CodeLYY
Advisory CommitteeHO
DecisionUnknown

Device Summary

FAMILY FIRST AID KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technologies International, Inc.. It received FDA 510(k) clearance on 1994-03-23 under 510(k) number K935131. 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 FAMILY FIRST AID KIT?

FAMILY FIRST AID KIT is a medical device that received FDA 510(k) clearance on 1994-03-23. The listed applicant is Medical Technologies International, Inc.. The 510(k) number is K935131.

When did FAMILY FIRST AID KIT receive FDA 510(k) clearance?

FAMILY FIRST AID KIT received FDA 510(k) clearance on 1994-03-23, under 510(k) number K935131.

Who is the listed applicant for FAMILY FIRST AID KIT?

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

What is the FDA product code for FAMILY FIRST AID KIT?

The FDA product code for FAMILY FIRST AID KIT is LYY.

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 Medical Technologies International, 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: LYY)

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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