MODEL G-61 ULTRASONIC DENTAL UNIT
K-Number: K791585 · 1979-09-19
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Device Summary
Frequently Asked Questions
What is the MODEL G-61 ULTRASONIC DENTAL UNIT?
MODEL G-61 ULTRASONIC DENTAL UNIT is a medical device that received FDA 510(k) clearance on 1979-09-19. The listed applicant is Cavitron Corp.. The 510(k) number is K791585.
When did MODEL G-61 ULTRASONIC DENTAL UNIT receive FDA 510(k) clearance?
MODEL G-61 ULTRASONIC DENTAL UNIT received FDA 510(k) clearance on 1979-09-19, under 510(k) number K791585.
Who is the listed applicant for MODEL G-61 ULTRASONIC DENTAL UNIT?
The FDA 510(k) record lists Cavitron Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL G-61 ULTRASONIC DENTAL UNIT?
The FDA product code for MODEL G-61 ULTRASONIC DENTAL UNIT is ELC.
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 Cavitron 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: ELC)
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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