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FDA 510(k)

EZZIE SYSTEM

K-Number: K851740 · 1985-07-15

Decision Date1985-07-15
Product CodeIQA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EZZIE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Independent Living, Inc.. It received FDA 510(k) clearance on 1985-07-15 under 510(k) number K851740. The device is classified under product code IQA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZZIE SYSTEM?

EZZIE SYSTEM is a medical device that received FDA 510(k) clearance on 1985-07-15. The listed applicant is Independent Living, Inc.. The 510(k) number is K851740.

When did EZZIE SYSTEM receive FDA 510(k) clearance?

EZZIE SYSTEM received FDA 510(k) clearance on 1985-07-15, under 510(k) number K851740.

Who is the listed applicant for EZZIE SYSTEM?

The FDA 510(k) record lists Independent Living, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZZIE SYSTEM?

The FDA product code for EZZIE SYSTEM is IQA.

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.

Related Devices (Code: IQA)

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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