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FDA 510(k)

INTRAORAL DENTAL X-RAY GENERATOR

K-Number: K780742 · 1978-07-27

ApplicantSiemens Corp.
Decision Date1978-07-27
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTRAORAL DENTAL X-RAY GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1978-07-27 under 510(k) number K780742. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 66 devices →

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.

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