TACAMO MANUAL WHEELCHAIR
K-Number: K101719 · 2010-08-25
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Device Summary
Frequently Asked Questions
What is the TACAMO MANUAL WHEELCHAIR?
TACAMO MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2010-08-25. The listed applicant is Dalton Instrument Corp.. The 510(k) number is K101719.
When did TACAMO MANUAL WHEELCHAIR receive FDA 510(k) clearance?
TACAMO MANUAL WHEELCHAIR received FDA 510(k) clearance on 2010-08-25, under 510(k) number K101719.
Who is the listed applicant for TACAMO MANUAL WHEELCHAIR?
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 TACAMO MANUAL WHEELCHAIR?
The FDA product code for TACAMO MANUAL WHEELCHAIR 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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