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FDA 510(k)

ASSERACHROM IX:AG

K-Number: K854312 · 1986-02-04

ApplicantAmerican Bioproducts Co.
Decision Date1986-02-04
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ASSERACHROM IX:AG 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 1986-02-04 under 510(k) number K854312. 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 IX:AG?

ASSERACHROM IX:AG is a medical device that received FDA 510(k) clearance on 1986-02-04. The listed applicant is American Bioproducts Co.. The 510(k) number is K854312.

When did ASSERACHROM IX:AG receive FDA 510(k) clearance?

ASSERACHROM IX:AG received FDA 510(k) clearance on 1986-02-04, under 510(k) number K854312.

Who is the listed applicant for ASSERACHROM IX:AG?

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 IX:AG?

The FDA product code for ASSERACHROM IX:AG is GGP.

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Other records listing American Bioproducts Co. as applicant

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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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