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FDA 510(k)

ASSERACHROM PROTEIN S TEST KIT

K-Number: K872479 · 1987-08-21

ApplicantAmerican Bioproducts Co.
Decision Date1987-08-21
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ASSERACHROM PROTEIN S TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Bioproducts Co.. It received FDA 510(k) clearance on 1987-08-21 under 510(k) number K872479. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASSERACHROM PROTEIN S TEST KIT?

ASSERACHROM PROTEIN S TEST KIT is a medical device that received FDA 510(k) clearance on 1987-08-21. The listed applicant is American Bioproducts Co.. The 510(k) number is K872479.

When did ASSERACHROM PROTEIN S TEST KIT receive FDA 510(k) clearance?

ASSERACHROM PROTEIN S TEST KIT received FDA 510(k) clearance on 1987-08-21, under 510(k) number K872479.

Who is the listed applicant for ASSERACHROM PROTEIN S TEST KIT?

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

What is the FDA product code for ASSERACHROM PROTEIN S TEST KIT?

The FDA product code for ASSERACHROM PROTEIN S TEST KIT is GGP.

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Other records listing American Bioproducts Co. as applicant

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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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