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FDA 510(k)

Playground For All Love Sesh

K-Number: K222567 · 2023-01-30

ApplicantPlayground For All
Decision Date2023-01-30
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Playground For All Love Sesh is the device name listed in this FDA 510(k) record. The listed applicant is Playground For All. It received FDA 510(k) clearance on 2023-01-30 under 510(k) number K222567. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Playground For All Love Sesh?

Playground For All Love Sesh is a medical device that received FDA 510(k) clearance on 2023-01-30. The listed applicant is Playground For All. The 510(k) number is K222567.

When did Playground For All Love Sesh receive FDA 510(k) clearance?

Playground For All Love Sesh received FDA 510(k) clearance on 2023-01-30, under 510(k) number K222567.

Who is the listed applicant for Playground For All Love Sesh?

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

What is the FDA product code for Playground For All Love Sesh?

The FDA product code for Playground For All Love Sesh is NUC.

Related Devices (Code: NUC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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