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FDA 510(k)

CENTRIFICHEM ALBUMIN

K-Number: K802436 · 1980-10-31

ApplicantUnion Carbide Corp.
Decision Date1980-10-31
Product CodeCIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIFICHEM ALBUMIN 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 1980-10-31 under 510(k) number K802436. The device is classified under product code CIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIFICHEM ALBUMIN?

CENTRIFICHEM ALBUMIN is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is Union Carbide Corp.. The 510(k) number is K802436.

When did CENTRIFICHEM ALBUMIN receive FDA 510(k) clearance?

CENTRIFICHEM ALBUMIN received FDA 510(k) clearance on 1980-10-31, under 510(k) number K802436.

Who is the listed applicant for CENTRIFICHEM ALBUMIN?

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 CENTRIFICHEM ALBUMIN?

The FDA product code for CENTRIFICHEM ALBUMIN is CIX.

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Other records listing Union Carbide Corp. as applicant

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Related Devices (Code: CIX)

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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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