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FDA 510(k)

TEST, SLIDE FOR C-REATIVE PROTEIN

K-Number: K760354 · 1976-08-11

ApplicantIcl Scientific
Decision Date1976-08-11
Product CodeDCK
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TEST, SLIDE FOR C-REATIVE PROTEIN is the device name listed in this FDA 510(k) record. The listed applicant is Icl Scientific. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760354. 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 TEST, SLIDE FOR C-REATIVE PROTEIN?

TEST, SLIDE FOR C-REATIVE PROTEIN is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Icl Scientific. The 510(k) number is K760354.

When did TEST, SLIDE FOR C-REATIVE PROTEIN receive FDA 510(k) clearance?

TEST, SLIDE FOR C-REATIVE PROTEIN received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760354.

Who is the listed applicant for TEST, SLIDE FOR C-REATIVE PROTEIN?

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

What is the FDA product code for TEST, SLIDE FOR C-REATIVE PROTEIN?

The FDA product code for TEST, SLIDE FOR C-REATIVE PROTEIN is 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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