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FDA 510(k)

SIRECUST 311S

K-Number: K800593 · 1980-04-02

ApplicantSiemens Corp.
Decision Date1980-04-02
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIRECUST 311S is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1980-04-02 under 510(k) number K800593. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIRECUST 311S?

SIRECUST 311S is a medical device that received FDA 510(k) clearance on 1980-04-02. The listed applicant is Siemens Corp.. The 510(k) number is K800593.

When did SIRECUST 311S receive FDA 510(k) clearance?

SIRECUST 311S received FDA 510(k) clearance on 1980-04-02, under 510(k) number K800593.

Who is the listed applicant for SIRECUST 311S?

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 SIRECUST 311S?

The FDA product code for SIRECUST 311S is DPS.

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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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