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FDA 510(k)

FAIRY WORLD INC

K-Number: K951992 · 1995-06-06

ApplicantFairy World, Inc.
Decision Date1995-06-06
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FAIRY WORLD INC is the device name listed in this FDA 510(k) record. The listed applicant is Fairy World, Inc.. It received FDA 510(k) clearance on 1995-06-06 under 510(k) number K951992. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FAIRY WORLD INC?

FAIRY WORLD INC is a medical device that received FDA 510(k) clearance on 1995-06-06. The listed applicant is Fairy World, Inc.. The 510(k) number is K951992.

When did FAIRY WORLD INC receive FDA 510(k) clearance?

FAIRY WORLD INC received FDA 510(k) clearance on 1995-06-06, under 510(k) number K951992.

Who is the listed applicant for FAIRY WORLD INC?

The FDA 510(k) record lists Fairy World, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FAIRY WORLD INC?

The FDA product code for FAIRY WORLD INC is HQY.

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Related Devices (Code: HQY)

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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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