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FDA 510(k)

LIATEST PROTEIN S KIT

K-Number: K912468 · 1991-10-02

ApplicantAmerican Bioproducts Co.
Decision Date1991-10-02
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LIATEST PROTEIN S 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 1991-10-02 under 510(k) number K912468. 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 LIATEST PROTEIN S KIT?

LIATEST PROTEIN S KIT is a medical device that received FDA 510(k) clearance on 1991-10-02. The listed applicant is American Bioproducts Co.. The 510(k) number is K912468.

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

LIATEST PROTEIN S KIT received FDA 510(k) clearance on 1991-10-02, under 510(k) number K912468.

Who is the listed applicant for LIATEST PROTEIN S 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 LIATEST PROTEIN S KIT?

The FDA product code for LIATEST PROTEIN S 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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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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