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FDA 510(k)

SIEMENS-ELEMA PSA 376

K-Number: K812104 · 1981-12-02

ApplicantSiemens Corp.
Decision Date1981-12-02
Product CodeDTA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS-ELEMA PSA 376 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1981-12-02 under 510(k) number K812104. The device is classified under product code DTA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS-ELEMA PSA 376?

SIEMENS-ELEMA PSA 376 is a medical device that received FDA 510(k) clearance on 1981-12-02. The listed applicant is Siemens Corp.. The 510(k) number is K812104.

When did SIEMENS-ELEMA PSA 376 receive FDA 510(k) clearance?

SIEMENS-ELEMA PSA 376 received FDA 510(k) clearance on 1981-12-02, under 510(k) number K812104.

Who is the listed applicant for SIEMENS-ELEMA PSA 376?

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 SIEMENS-ELEMA PSA 376?

The FDA product code for SIEMENS-ELEMA PSA 376 is DTA.

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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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