KARECO INT'L WHEELCHAIR
K-Number: K843688 · 1984-11-23
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Device Summary
Frequently Asked Questions
What is the KARECO INT'L WHEELCHAIR?
KARECO INT'L WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1984-11-23. The listed applicant is Kareco Intl., Inc.. The 510(k) number is K843688.
When did KARECO INT'L WHEELCHAIR receive FDA 510(k) clearance?
KARECO INT'L WHEELCHAIR received FDA 510(k) clearance on 1984-11-23, under 510(k) number K843688.
Who is the listed applicant for KARECO INT'L WHEELCHAIR?
The FDA 510(k) record lists Kareco Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KARECO INT'L WHEELCHAIR?
The FDA product code for KARECO INT'L 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 Kareco Intl., 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: 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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