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FDA 510(k)

POLYPHOS 500

K-Number: K812616 · 1981-10-13

ApplicantSiemens Corp.
Decision Date1981-10-13
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POLYPHOS 500 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1981-10-13 under 510(k) number K812616. 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 POLYPHOS 500?

POLYPHOS 500 is a medical device that received FDA 510(k) clearance on 1981-10-13. The listed applicant is Siemens Corp.. The 510(k) number is K812616.

When did POLYPHOS 500 receive FDA 510(k) clearance?

POLYPHOS 500 received FDA 510(k) clearance on 1981-10-13, under 510(k) number K812616.

Who is the listed applicant for POLYPHOS 500?

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 POLYPHOS 500?

The FDA product code for POLYPHOS 500 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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