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FDA 510(k)

POWER PROCESSOR SAMPLE PROCESSING SYSTEM WITH GENERIC CONNECTIONS

K-Number: K110413 · 2011-05-11

ApplicantBeckman Coulter, Inc.
Decision Date2011-05-11
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

POWER PROCESSOR SAMPLE PROCESSING SYSTEM WITH GENERIC CONNECTIONS is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Coulter, Inc.. It received FDA 510(k) clearance on 2011-05-11 under 510(k) number K110413. The device is classified under product code CDD. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER PROCESSOR SAMPLE PROCESSING SYSTEM WITH GENERIC CONNECTIONS?

POWER PROCESSOR SAMPLE PROCESSING SYSTEM WITH GENERIC CONNECTIONS is a medical device that received FDA 510(k) clearance on 2011-05-11. The listed applicant is Beckman Coulter, Inc.. The 510(k) number is K110413.

When did POWER PROCESSOR SAMPLE PROCESSING SYSTEM WITH GENERIC CONNECTIONS receive FDA 510(k) clearance?

POWER PROCESSOR SAMPLE PROCESSING SYSTEM WITH GENERIC CONNECTIONS received FDA 510(k) clearance on 2011-05-11, under 510(k) number K110413.

Who is the listed applicant for POWER PROCESSOR SAMPLE PROCESSING SYSTEM WITH GENERIC CONNECTIONS?

The FDA 510(k) record lists Beckman Coulter, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWER PROCESSOR SAMPLE PROCESSING SYSTEM WITH GENERIC CONNECTIONS?

The FDA product code for POWER PROCESSOR SAMPLE PROCESSING SYSTEM WITH GENERIC CONNECTIONS is CDD.

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Related Devices (Code: CDD)

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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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