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FDA 510(k)

POLYDOROS IS

K-Number: K933240 · 1993-09-07

Decision Date1993-09-07
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POLYDOROS IS is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1993-09-07 under 510(k) number K933240. 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 POLYDOROS IS?

POLYDOROS IS is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K933240.

When did POLYDOROS IS receive FDA 510(k) clearance?

POLYDOROS IS received FDA 510(k) clearance on 1993-09-07, under 510(k) number K933240.

Who is the listed applicant for POLYDOROS IS?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POLYDOROS IS?

The FDA product code for POLYDOROS IS is IZO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Siemens Medical Solutions USA, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 732 devices →

Related Devices (Code: IZO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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