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FDA 510(k)

HAYFEVER HELMET

K-Number: K842973 · 1984-10-25

ApplicantR.H. Hinchli Fle & Sons, Ltd.
Decision Date1984-10-25
Product CodeFRF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HAYFEVER HELMET is the device name listed in this FDA 510(k) record. The listed applicant is R.H. Hinchli Fle & Sons, Ltd.. It received FDA 510(k) clearance on 1984-10-25 under 510(k) number K842973. The device is classified under product code FRF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAYFEVER HELMET?

HAYFEVER HELMET is a medical device that received FDA 510(k) clearance on 1984-10-25. The listed applicant is R.H. Hinchli Fle & Sons, Ltd.. The 510(k) number is K842973.

When did HAYFEVER HELMET receive FDA 510(k) clearance?

HAYFEVER HELMET received FDA 510(k) clearance on 1984-10-25, under 510(k) number K842973.

Who is the listed applicant for HAYFEVER HELMET?

The FDA 510(k) record lists R.H. Hinchli Fle & Sons, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAYFEVER HELMET?

The FDA product code for HAYFEVER HELMET is FRF.

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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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