ABLE GENERATION BOOSTER CHAIR
K-Number: K923750 · 1993-01-29
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Device Summary
Frequently Asked Questions
What is the ABLE GENERATION BOOSTER CHAIR?
ABLE GENERATION BOOSTER 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 K923750.
When did ABLE GENERATION BOOSTER CHAIR receive FDA 510(k) clearance?
ABLE GENERATION BOOSTER CHAIR received FDA 510(k) clearance on 1993-01-29, under 510(k) number K923750.
Who is the listed applicant for ABLE GENERATION BOOSTER 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 BOOSTER CHAIR?
The FDA product code for ABLE GENERATION BOOSTER 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.
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