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FDA 510(k)

SIEMENS POLYDOROS 800

K-Number: K820112 · 1982-02-24

ApplicantSiemens Corp.
Decision Date1982-02-24
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS POLYDOROS 800 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1982-02-24 under 510(k) number K820112. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS POLYDOROS 800?

SIEMENS POLYDOROS 800 is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is Siemens Corp.. The 510(k) number is K820112.

When did SIEMENS POLYDOROS 800 receive FDA 510(k) clearance?

SIEMENS POLYDOROS 800 received FDA 510(k) clearance on 1982-02-24, under 510(k) number K820112.

Who is the listed applicant for SIEMENS POLYDOROS 800?

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 POLYDOROS 800?

The FDA product code for SIEMENS POLYDOROS 800 is IZO.

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Related Devices (Code: IZO)

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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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