FDA 510(k)

TINA-QUANT CRP

K-Number: K930621 · 1993-03-10

Decision Date1993-03-10

Product CodeDCK

Advisory CommitteeIM

DecisionSubstantially Equivalent

Device Summary

TINA-QUANT CRP is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1993-03-10 under 510(k) number K930621. 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 TINA-QUANT CRP?

TINA-QUANT CRP is a medical device that received FDA 510(k) clearance on 1993-03-10. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K930621.

When did TINA-QUANT CRP receive FDA 510(k) clearance?

TINA-QUANT CRP received FDA 510(k) clearance on 1993-03-10, under 510(k) number K930621.

Who is the listed applicant for TINA-QUANT CRP?

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

What is the FDA product code for TINA-QUANT CRP?

The FDA product code for TINA-QUANT CRP is DCK.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.