7.5 MHZ WP TRANSDUCER
K-Number: K810748 · 1981-06-19
Advertisement
Device Summary
Frequently Asked Questions
What is the 7.5 MHZ WP TRANSDUCER?
7.5 MHZ WP TRANSDUCER is a medical device that received FDA 510(k) clearance on 1981-06-19. The listed applicant is General Electric Co.. The 510(k) number is K810748.
When did 7.5 MHZ WP TRANSDUCER receive FDA 510(k) clearance?
7.5 MHZ WP TRANSDUCER received FDA 510(k) clearance on 1981-06-19, under 510(k) number K810748.
Who is the listed applicant for 7.5 MHZ WP 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 7.5 MHZ WP TRANSDUCER?
The FDA product code for 7.5 MHZ WP 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.
Advertisement