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FDA 510(k)

ACCUTNI QC ON THE ACCESS IMMUNOASSAY SYSTEM #33349

K-Number: K010428 · 2001-03-13

ApplicantBeckman Coulter, Inc.
Decision Date2001-03-13
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACCUTNI QC ON THE ACCESS IMMUNOASSAY SYSTEM #33349 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 2001-03-13 under 510(k) number K010428. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUTNI QC ON THE ACCESS IMMUNOASSAY SYSTEM #33349?

ACCUTNI QC ON THE ACCESS IMMUNOASSAY SYSTEM #33349 is a medical device that received FDA 510(k) clearance on 2001-03-13. The listed applicant is Beckman Coulter, Inc.. The 510(k) number is K010428.

When did ACCUTNI QC ON THE ACCESS IMMUNOASSAY SYSTEM #33349 receive FDA 510(k) clearance?

ACCUTNI QC ON THE ACCESS IMMUNOASSAY SYSTEM #33349 received FDA 510(k) clearance on 2001-03-13, under 510(k) number K010428.

Who is the listed applicant for ACCUTNI QC ON THE ACCESS IMMUNOASSAY SYSTEM #33349?

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 ACCUTNI QC ON THE ACCESS IMMUNOASSAY SYSTEM #33349?

The FDA product code for ACCUTNI QC ON THE ACCESS IMMUNOASSAY SYSTEM #33349 is JJX.

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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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