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FDA 510(k)

KF-101-07 DIALYZER

K-Number: K822337 · 1983-02-16

Decision Date1983-02-16
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KF-101-07 DIALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Extracorporeal Medical Specialities, Inc.. It received FDA 510(k) clearance on 1983-02-16 under 510(k) number K822337. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KF-101-07 DIALYZER?

KF-101-07 DIALYZER is a medical device that received FDA 510(k) clearance on 1983-02-16. The listed applicant is Extracorporeal Medical Specialities, Inc.. The 510(k) number is K822337.

When did KF-101-07 DIALYZER receive FDA 510(k) clearance?

KF-101-07 DIALYZER received FDA 510(k) clearance on 1983-02-16, under 510(k) number K822337.

Who is the listed applicant for KF-101-07 DIALYZER?

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

What is the FDA product code for KF-101-07 DIALYZER?

The FDA product code for KF-101-07 DIALYZER is KOC.

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 Extracorporeal Medical Specialities, 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.

View all 69 devices →

Related Devices (Code: KOC)

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

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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