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FDA 510(k)

ALIZARIN SULFONATE, CALCIUM

K-Number: K801290 · 1980-06-30

ApplicantUnion Carbide Corp.
Decision Date1980-06-30
Product CodeCID
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ALIZARIN SULFONATE, CALCIUM is the device name listed in this FDA 510(k) record. The listed applicant is Union Carbide Corp.. It received FDA 510(k) clearance on 1980-06-30 under 510(k) number K801290. The device is classified under product code CID. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALIZARIN SULFONATE, CALCIUM?

ALIZARIN SULFONATE, CALCIUM is a medical device that received FDA 510(k) clearance on 1980-06-30. The listed applicant is Union Carbide Corp.. The 510(k) number is K801290.

When did ALIZARIN SULFONATE, CALCIUM receive FDA 510(k) clearance?

ALIZARIN SULFONATE, CALCIUM received FDA 510(k) clearance on 1980-06-30, under 510(k) number K801290.

Who is the listed applicant for ALIZARIN SULFONATE, CALCIUM?

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

What is the FDA product code for ALIZARIN SULFONATE, CALCIUM?

The FDA product code for ALIZARIN SULFONATE, CALCIUM is CID.

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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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