DALTON FOLDING WHEELCHAIRS
K-Number: K850178 · 1985-04-25
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Device Summary
Frequently Asked Questions
What is the DALTON FOLDING WHEELCHAIRS?
DALTON FOLDING WHEELCHAIRS is a medical device that received FDA 510(k) clearance on 1985-04-25. The listed applicant is Dalton Instrument Corp.. The 510(k) number is K850178.
When did DALTON FOLDING WHEELCHAIRS receive FDA 510(k) clearance?
DALTON FOLDING WHEELCHAIRS received FDA 510(k) clearance on 1985-04-25, under 510(k) number K850178.
Who is the listed applicant for DALTON FOLDING WHEELCHAIRS?
The FDA 510(k) record lists Dalton Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DALTON FOLDING WHEELCHAIRS?
The FDA product code for DALTON FOLDING WHEELCHAIRS 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 Dalton Instrument 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.
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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