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FDA 510(k)

AKI COMPACS DATA COMPRESION MODULE FOR DIAGNOSTIC IMAGES

K-Number: K963610 · 1996-11-27

Decision Date1996-11-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AKI COMPACS DATA COMPRESION MODULE FOR DIAGNOSTIC IMAGES is the device name listed in this FDA 510(k) record. The listed applicant is A.L.I. Technologies, Inc.. It received FDA 510(k) clearance on 1996-11-27 under 510(k) number K963610. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AKI COMPACS DATA COMPRESION MODULE FOR DIAGNOSTIC IMAGES?

AKI COMPACS DATA COMPRESION MODULE FOR DIAGNOSTIC IMAGES is a medical device that received FDA 510(k) clearance on 1996-11-27. The listed applicant is A.L.I. Technologies, Inc.. The 510(k) number is K963610.

When did AKI COMPACS DATA COMPRESION MODULE FOR DIAGNOSTIC IMAGES receive FDA 510(k) clearance?

AKI COMPACS DATA COMPRESION MODULE FOR DIAGNOSTIC IMAGES received FDA 510(k) clearance on 1996-11-27, under 510(k) number K963610.

Who is the listed applicant for AKI COMPACS DATA COMPRESION MODULE FOR DIAGNOSTIC IMAGES?

The FDA 510(k) record lists A.L.I. Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AKI COMPACS DATA COMPRESION MODULE FOR DIAGNOSTIC IMAGES?

The FDA product code for AKI COMPACS DATA COMPRESION MODULE FOR DIAGNOSTIC IMAGES is LLZ.

Related Clinical Trials

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.

Other records listing A.L.I. Technologies, Inc. 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.

Related Devices (Code: LLZ)

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.

Official Source

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