INTRAORAL DENTAL X-RAY GENERATOR
K-Number: K780742 · 1978-07-27
Advertisement
Device Summary
Frequently Asked Questions
What is the INTRAORAL DENTAL X-RAY GENERATOR?
INTRAORAL DENTAL X-RAY GENERATOR is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is Siemens Corp.. The 510(k) number is K780742.
When did INTRAORAL DENTAL X-RAY GENERATOR receive FDA 510(k) clearance?
INTRAORAL DENTAL X-RAY GENERATOR received FDA 510(k) clearance on 1978-07-27, under 510(k) number K780742.
Who is the listed applicant for INTRAORAL DENTAL X-RAY GENERATOR?
The FDA 510(k) record lists Siemens Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRAORAL DENTAL X-RAY GENERATOR?
The FDA product code for INTRAORAL DENTAL X-RAY GENERATOR is IZO.
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 Siemens 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: IZO)
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