BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6
K-Number: K070611 · 2007-07-11
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Device Summary
Frequently Asked Questions
What is the BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6?
BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6 is a medical device that received FDA 510(k) clearance on 2007-07-11. The listed applicant is Nomos Corp.. The 510(k) number is K070611.
When did BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6 receive FDA 510(k) clearance?
BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6 received FDA 510(k) clearance on 2007-07-11, under 510(k) number K070611.
Who is the listed applicant for BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6?
The FDA 510(k) record lists Nomos Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6?
The FDA product code for BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6 is IYE.
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 Nomos Corp. 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: IYE)
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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