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FDA 510(k)

DR. HESSEL'S INSECT POISON REMOVER

K-Number: K844048 · 1985-01-23

ApplicantMedie Group
Decision Date1985-01-23
Product CodeKYP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DR. HESSEL'S INSECT POISON REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Medie Group. It received FDA 510(k) clearance on 1985-01-23 under 510(k) number K844048. The device is classified under product code KYP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DR. HESSEL'S INSECT POISON REMOVER?

DR. HESSEL'S INSECT POISON REMOVER is a medical device that received FDA 510(k) clearance on 1985-01-23. The listed applicant is Medie Group. The 510(k) number is K844048.

When did DR. HESSEL'S INSECT POISON REMOVER receive FDA 510(k) clearance?

DR. HESSEL'S INSECT POISON REMOVER received FDA 510(k) clearance on 1985-01-23, under 510(k) number K844048.

Who is the listed applicant for DR. HESSEL'S INSECT POISON REMOVER?

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

What is the FDA product code for DR. HESSEL'S INSECT POISON REMOVER?

The FDA product code for DR. HESSEL'S INSECT POISON REMOVER is KYP.

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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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