FINGER COT
K-Number: K820383 · 1982-02-24
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Device Summary
Frequently Asked Questions
What is the FINGER COT?
FINGER COT is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is Conco Medical Co.. The 510(k) number is K820383.
When did FINGER COT receive FDA 510(k) clearance?
FINGER COT received FDA 510(k) clearance on 1982-02-24, under 510(k) number K820383.
Who is the listed applicant for FINGER COT?
The FDA 510(k) record lists Conco Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FINGER COT?
The FDA product code for FINGER COT is ILH.
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 Conco Medical Co. 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: ILH)
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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