Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ABLE GENERATION PLAY CHAIR

K-Number: K923752 · 1993-01-29

Decision Date1993-01-29
Product CodeINN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ABLE GENERATION PLAY CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is The Able Generation, Inc.. It received FDA 510(k) clearance on 1993-01-29 under 510(k) number K923752. The device is classified under product code INN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABLE GENERATION PLAY CHAIR?

ABLE GENERATION PLAY CHAIR is a medical device that received FDA 510(k) clearance on 1993-01-29. The listed applicant is The Able Generation, Inc.. The 510(k) number is K923752.

When did ABLE GENERATION PLAY CHAIR receive FDA 510(k) clearance?

ABLE GENERATION PLAY CHAIR received FDA 510(k) clearance on 1993-01-29, under 510(k) number K923752.

Who is the listed applicant for ABLE GENERATION PLAY CHAIR?

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

What is the FDA product code for ABLE GENERATION PLAY CHAIR?

The FDA product code for ABLE GENERATION PLAY CHAIR is INN.

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 The Able Generation, Inc. 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.

Related Devices (Code: INN)

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.

↑