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FDA 510(k)

TINA-QUANT(R) (A) C3

K-Number: K870930 · 1987-03-24

ApplicantBoehringer Mannheim Corp.
Decision Date1987-03-24
Product CodeCZM
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TINA-QUANT(R) (A) C3 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 1987-03-24 under 510(k) number K870930. The device is classified under product code CZM. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TINA-QUANT(R) (A) C3?

TINA-QUANT(R) (A) C3 is a medical device that received FDA 510(k) clearance on 1987-03-24. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K870930.

When did TINA-QUANT(R) (A) C3 receive FDA 510(k) clearance?

TINA-QUANT(R) (A) C3 received FDA 510(k) clearance on 1987-03-24, under 510(k) number K870930.

Who is the listed applicant for TINA-QUANT(R) (A) C3?

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(R) (A) C3?

The FDA product code for TINA-QUANT(R) (A) C3 is CZM.

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Other records listing Boehringer Mannheim Corp. as applicant

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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.

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