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FDA 510(k)

STACHROM VIII:C TEST KIT

K-Number: K874097 · 1987-12-03

ApplicantAmerican Bioproducts Co.
Decision Date1987-12-03
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

STACHROM VIII:C 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 1987-12-03 under 510(k) number K874097. 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 STACHROM VIII:C TEST KIT?

STACHROM VIII:C TEST KIT is a medical device that received FDA 510(k) clearance on 1987-12-03. The listed applicant is American Bioproducts Co.. The 510(k) number is K874097.

When did STACHROM VIII:C TEST KIT receive FDA 510(k) clearance?

STACHROM VIII:C TEST KIT received FDA 510(k) clearance on 1987-12-03, under 510(k) number K874097.

Who is the listed applicant for STACHROM VIII:C 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 STACHROM VIII:C TEST KIT?

The FDA product code for STACHROM VIII:C TEST KIT is GGP.

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Other records listing American Bioproducts Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: GGP)

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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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