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FDA 510(k)

PLAYSKOOL

K-Number: K955069 · 1995-12-22

ApplicantHasbro, Inc.
Decision Date1995-12-22
Product CodeKKO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PLAYSKOOL is the device name listed in this FDA 510(k) record. The listed applicant is Hasbro, Inc.. It received FDA 510(k) clearance on 1995-12-22 under 510(k) number K955069. The device is classified under product code KKO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLAYSKOOL?

PLAYSKOOL is a medical device that received FDA 510(k) clearance on 1995-12-22. The listed applicant is Hasbro, Inc.. The 510(k) number is K955069.

When did PLAYSKOOL receive FDA 510(k) clearance?

PLAYSKOOL received FDA 510(k) clearance on 1995-12-22, under 510(k) number K955069.

Who is the listed applicant for PLAYSKOOL?

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

What is the FDA product code for PLAYSKOOL?

The FDA product code for PLAYSKOOL is KKO.

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Related Devices (Code: KKO)

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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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