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FDA 510(k)

KAGER TRAPDUST

K-Number: K790085 · 1979-05-29

ApplicantKager Intl.
Decision Date1979-05-29
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KAGER TRAPDUST is the device name listed in this FDA 510(k) record. The listed applicant is Kager Intl.. It received FDA 510(k) clearance on 1979-05-29 under 510(k) number K790085. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAGER TRAPDUST?

KAGER TRAPDUST is a medical device that received FDA 510(k) clearance on 1979-05-29. The listed applicant is Kager Intl.. The 510(k) number is K790085.

When did KAGER TRAPDUST receive FDA 510(k) clearance?

KAGER TRAPDUST received FDA 510(k) clearance on 1979-05-29, under 510(k) number K790085.

Who is the listed applicant for KAGER TRAPDUST?

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

What is the FDA product code for KAGER TRAPDUST?

The FDA product code for KAGER TRAPDUST is LDQ.

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Related Devices (Code: LDQ)

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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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