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FDA 510(k)

BURNSHIELD FIRE BLANKET

K-Number: K921470 · 1993-04-20

Decision Date1993-04-20
Product CodeFPY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BURNSHIELD FIRE BLANKET is the device name listed in this FDA 510(k) record. The listed applicant is Levtrade Intl. (Pty) , Ltd.. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K921470. The device is classified under product code FPY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURNSHIELD FIRE BLANKET?

BURNSHIELD FIRE BLANKET is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Levtrade Intl. (Pty) , Ltd.. The 510(k) number is K921470.

When did BURNSHIELD FIRE BLANKET receive FDA 510(k) clearance?

BURNSHIELD FIRE BLANKET received FDA 510(k) clearance on 1993-04-20, under 510(k) number K921470.

Who is the listed applicant for BURNSHIELD FIRE BLANKET?

The FDA 510(k) record lists Levtrade Intl. (Pty) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BURNSHIELD FIRE BLANKET?

The FDA product code for BURNSHIELD FIRE BLANKET is FPY.

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 Levtrade Intl. (Pty) , Ltd. 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: FPY)

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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