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FDA 510(k)

TRIDOROS 712

K-Number: K791214 · 1979-07-30

ApplicantSiemens Corp.
Decision Date1979-07-30
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRIDOROS 712 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K791214. 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 TRIDOROS 712?

TRIDOROS 712 is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Siemens Corp.. The 510(k) number is K791214.

When did TRIDOROS 712 receive FDA 510(k) clearance?

TRIDOROS 712 received FDA 510(k) clearance on 1979-07-30, under 510(k) number K791214.

Who is the listed applicant for TRIDOROS 712?

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 TRIDOROS 712?

The FDA product code for TRIDOROS 712 is IZO.

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Related Devices (Code: IZO)

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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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