CYBER III OPTION UM, UC312, UC10, UCIC
K-Number: K955359 · 1995-12-19
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Device Summary
Frequently Asked Questions
What is the CYBER III OPTION UM, UC312, UC10, UCIC?
CYBER III OPTION UM, UC312, UC10, UCIC is a medical device that received FDA 510(k) clearance on 1995-12-19. The listed applicant is Qualitone. The 510(k) number is K955359.
When did CYBER III OPTION UM, UC312, UC10, UCIC receive FDA 510(k) clearance?
CYBER III OPTION UM, UC312, UC10, UCIC received FDA 510(k) clearance on 1995-12-19, under 510(k) number K955359.
Who is the listed applicant for CYBER III OPTION UM, UC312, UC10, UCIC?
The FDA 510(k) record lists Qualitone as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CYBER III OPTION UM, UC312, UC10, UCIC?
The FDA product code for CYBER III OPTION UM, UC312, UC10, UCIC is ESD.
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 Qualitone 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: ESD)
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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