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FDA 510(k)

AKS II

K-Number: K895095 · 1990-02-09

ApplicantAmoco Technology Co.
Decision Date1990-02-09
Product CodeLNJ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

AKS II is the device name listed in this FDA 510(k) record. The listed applicant is Amoco Technology Co.. It received FDA 510(k) clearance on 1990-02-09 under 510(k) number K895095. The device is classified under product code LNJ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AKS II?

AKS II is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is Amoco Technology Co.. The 510(k) number is K895095.

When did AKS II receive FDA 510(k) clearance?

AKS II received FDA 510(k) clearance on 1990-02-09, under 510(k) number K895095.

Who is the listed applicant for AKS II?

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

What is the FDA product code for AKS II?

The FDA product code for AKS II is LNJ.

Related Devices (Code: LNJ)

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.

K050236FISHVIEWApplied Spectral Imaging , Ltd.K012103BANDVIEW SYSTEMApplied Spectral Imaging , Ltd.K940240IKAROSMetasystems GmbHK912085ACLAIMS-ISW-TechnologyK902311GENEVISION - COMPUTER ASSISTED CHROMOSOME KARYO.Applied Imaging Corp.K872755KARYOTEC 100Amcor Electronics, Ltd.

Official Source

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