5 MHZ TRANSDUCER
K-Number: K810749 · 1981-04-17
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Device Summary
Frequently Asked Questions
What is the 5 MHZ TRANSDUCER?
5 MHZ TRANSDUCER is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is General Electric Co.. The 510(k) number is K810749.
When did 5 MHZ TRANSDUCER receive FDA 510(k) clearance?
5 MHZ TRANSDUCER received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810749.
Who is the listed applicant for 5 MHZ TRANSDUCER?
The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 5 MHZ TRANSDUCER?
The FDA product code for 5 MHZ TRANSDUCER is ITX.
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 General Electric 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: ITX)
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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