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FDA 510(k)

KIDS ROCK 3 CHAIR

K-Number: K111739 · 2011-08-12

Decision Date2011-08-12
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KIDS ROCK 3 CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Pride Mobility Products Corp.. It received FDA 510(k) clearance on 2011-08-12 under 510(k) number K111739. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIDS ROCK 3 CHAIR?

KIDS ROCK 3 CHAIR is a medical device that received FDA 510(k) clearance on 2011-08-12. The listed applicant is Pride Mobility Products Corp.. The 510(k) number is K111739.

When did KIDS ROCK 3 CHAIR receive FDA 510(k) clearance?

KIDS ROCK 3 CHAIR received FDA 510(k) clearance on 2011-08-12, under 510(k) number K111739.

Who is the listed applicant for KIDS ROCK 3 CHAIR?

The FDA 510(k) record lists Pride Mobility Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIDS ROCK 3 CHAIR?

The FDA product code for KIDS ROCK 3 CHAIR is IOR.

Related Clinical Trials

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.

Other records listing Pride Mobility Products Corp. as applicant

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.

View all 20 devices →

Related Devices (Code: IOR)

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.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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