COMBISON 200 & COMBISON 202
K-Number: K800094 · 1980-02-11
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Device Summary
Frequently Asked Questions
What is the COMBISON 200 & COMBISON 202?
COMBISON 200 & COMBISON 202 is a medical device that received FDA 510(k) clearance on 1980-02-11. The listed applicant is Kt Medical, Inc.. The 510(k) number is K800094.
When did COMBISON 200 & COMBISON 202 receive FDA 510(k) clearance?
COMBISON 200 & COMBISON 202 received FDA 510(k) clearance on 1980-02-11, under 510(k) number K800094.
Who is the listed applicant for COMBISON 200 & COMBISON 202?
The FDA 510(k) record lists Kt Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMBISON 200 & COMBISON 202?
The FDA product code for COMBISON 200 & COMBISON 202 is IYO.
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 Kt Medical, 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: IYO)
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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