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FDA 510(k)

SIEMENS SIRESKOP 4

K-Number: K820111 · 1982-02-18

ApplicantSiemens Corp.
Decision Date1982-02-18
Product CodeKXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS SIRESKOP 4 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1982-02-18 under 510(k) number K820111. The device is classified under product code KXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS SIRESKOP 4?

SIEMENS SIRESKOP 4 is a medical device that received FDA 510(k) clearance on 1982-02-18. The listed applicant is Siemens Corp.. The 510(k) number is K820111.

When did SIEMENS SIRESKOP 4 receive FDA 510(k) clearance?

SIEMENS SIRESKOP 4 received FDA 510(k) clearance on 1982-02-18, under 510(k) number K820111.

Who is the listed applicant for SIEMENS SIRESKOP 4?

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 SIRESKOP 4?

The FDA product code for SIEMENS SIRESKOP 4 is KXJ.

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Other records listing Siemens Corp. as applicant

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Related Devices (Code: KXJ)

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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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