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FDA 510(k)

CERASORB PLUS

K-Number: K120152 · 2012-08-13

ApplicantRiemser Arzneimittel AG
Decision Date2012-08-13
Product CodeNPM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERASORB PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Riemser Arzneimittel AG. It received FDA 510(k) clearance on 2012-08-13 under 510(k) number K120152. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERASORB PLUS?

CERASORB PLUS is a medical device that received FDA 510(k) clearance on 2012-08-13. The listed applicant is Riemser Arzneimittel AG. The 510(k) number is K120152.

When did CERASORB PLUS receive FDA 510(k) clearance?

CERASORB PLUS received FDA 510(k) clearance on 2012-08-13, under 510(k) number K120152.

Who is the listed applicant for CERASORB PLUS?

The FDA 510(k) record lists Riemser Arzneimittel AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERASORB PLUS?

The FDA product code for CERASORB PLUS is NPM.

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Other records listing Riemser Arzneimittel AG 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.

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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.

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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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