COMBISON 301 PW ULTRASOUND SYSTEM AND TRANSDUCERS
K-Number: K002491 · 2000-08-25
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Device Summary
Frequently Asked Questions
What is the COMBISON 301 PW ULTRASOUND SYSTEM AND TRANSDUCERS?
COMBISON 301 PW ULTRASOUND SYSTEM AND TRANSDUCERS is a medical device that received FDA 510(k) clearance on 2000-08-25. The listed applicant is Medison Co., Ltd.. The 510(k) number is K002491.
When did COMBISON 301 PW ULTRASOUND SYSTEM AND TRANSDUCERS receive FDA 510(k) clearance?
COMBISON 301 PW ULTRASOUND SYSTEM AND TRANSDUCERS received FDA 510(k) clearance on 2000-08-25, under 510(k) number K002491.
Who is the listed applicant for COMBISON 301 PW ULTRASOUND SYSTEM AND TRANSDUCERS?
The FDA 510(k) record lists Medison Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMBISON 301 PW ULTRASOUND SYSTEM AND TRANSDUCERS?
The FDA product code for COMBISON 301 PW ULTRASOUND SYSTEM AND TRANSDUCERS is IYN.
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 Medison Co., Ltd. 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: IYN)
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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