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FDA 510(k)

SIRCAM 103

K-Number: K810191 · 1981-02-26

ApplicantSiemens Corp.
Decision Date1981-02-26
Product CodeIZJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIRCAM 103 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1981-02-26 under 510(k) number K810191. The device is classified under product code IZJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIRCAM 103?

SIRCAM 103 is a medical device that received FDA 510(k) clearance on 1981-02-26. The listed applicant is Siemens Corp.. The 510(k) number is K810191.

When did SIRCAM 103 receive FDA 510(k) clearance?

SIRCAM 103 received FDA 510(k) clearance on 1981-02-26, under 510(k) number K810191.

Who is the listed applicant for SIRCAM 103?

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 SIRCAM 103?

The FDA product code for SIRCAM 103 is IZJ.

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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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