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FDA 510(k)

FIRST AID KIT

K-Number: K921976 · 1992-09-10

ApplicantThe Home Emergency Room
Decision Date1992-09-10
Product CodeLYY
Advisory CommitteeHO
DecisionUnknown

Device Summary

FIRST AID KIT is the device name listed in this FDA 510(k) record. The listed applicant is The Home Emergency Room. It received FDA 510(k) clearance on 1992-09-10 under 510(k) number K921976. 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 FIRST AID KIT?

FIRST AID KIT is a medical device that received FDA 510(k) clearance on 1992-09-10. The listed applicant is The Home Emergency Room. The 510(k) number is K921976.

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

FIRST AID KIT received FDA 510(k) clearance on 1992-09-10, under 510(k) number K921976.

Who is the listed applicant for FIRST AID KIT?

The FDA 510(k) record lists The Home Emergency Room as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIRST AID KIT?

The FDA product code for FIRST AID KIT is LYY.

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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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