FDA 510(k)

K-AID

K-Number: K820150 · 1982-01-29

Decision Date1982-01-29

Product CodeKPO

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

K-AID is the device name listed in this FDA 510(k) record. The listed applicant is Sytek Laboratories. It received FDA 510(k) clearance on 1982-01-29 under 510(k) number K820150. The device is classified under product code KPO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-AID?

K-AID is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is Sytek Laboratories. The 510(k) number is K820150.

When did K-AID receive FDA 510(k) clearance?

K-AID received FDA 510(k) clearance on 1982-01-29, under 510(k) number K820150.

Who is the listed applicant for K-AID?

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

What is the FDA product code for K-AID?

The FDA product code for K-AID is KPO.

Related Devices (Code: KPO)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.