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FDA 510(k)

VISION(R) CRP

K-Number: K875345 · 1988-03-21

ApplicantAbbott Laboratories
Decision Date1988-03-21
Product CodeDCK
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

VISION(R) CRP is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1988-03-21 under 510(k) number K875345. The device is classified under product code DCK. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISION(R) CRP?

VISION(R) CRP is a medical device that received FDA 510(k) clearance on 1988-03-21. The listed applicant is Abbott Laboratories. The 510(k) number is K875345.

When did VISION(R) CRP receive FDA 510(k) clearance?

VISION(R) CRP received FDA 510(k) clearance on 1988-03-21, under 510(k) number K875345.

Who is the listed applicant for VISION(R) CRP?

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

What is the FDA product code for VISION(R) CRP?

The FDA product code for VISION(R) CRP is DCK.

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Related Devices (Code: DCK)

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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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