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FDA 510(k)

SIROPORT

K-Number: K800172 · 1980-02-05

ApplicantSiemens Corp.
Decision Date1980-02-05
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SIROPORT is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1980-02-05 under 510(k) number K800172. The device is classified under product code KLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIROPORT?

SIROPORT is a medical device that received FDA 510(k) clearance on 1980-02-05. The listed applicant is Siemens Corp.. The 510(k) number is K800172.

When did SIROPORT receive FDA 510(k) clearance?

SIROPORT received FDA 510(k) clearance on 1980-02-05, under 510(k) number K800172.

Who is the listed applicant for SIROPORT?

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 SIROPORT?

The FDA product code for SIROPORT is KLC.

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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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