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FDA 510(k)

HAYDAY IRRIT-EASER WAND

K-Number: K840035 · 1984-01-30

ApplicantHayday Irrit-Easer
Decision Date1984-01-30
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HAYDAY IRRIT-EASER WAND is the device name listed in this FDA 510(k) record. The listed applicant is Hayday Irrit-Easer. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K840035. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAYDAY IRRIT-EASER WAND?

HAYDAY IRRIT-EASER WAND is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Hayday Irrit-Easer. The 510(k) number is K840035.

When did HAYDAY IRRIT-EASER WAND receive FDA 510(k) clearance?

HAYDAY IRRIT-EASER WAND received FDA 510(k) clearance on 1984-01-30, under 510(k) number K840035.

Who is the listed applicant for HAYDAY IRRIT-EASER WAND?

The FDA 510(k) record lists Hayday Irrit-Easer as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAYDAY IRRIT-EASER WAND?

The FDA product code for HAYDAY IRRIT-EASER WAND is ISA.

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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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