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FDA 510(k)

INPERSOL PERITONEAL DIALSIS CYCLER SET

K-Number: K823217 · 1982-11-30

Decision Date1982-11-30
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INPERSOL PERITONEAL DIALSIS CYCLER SET is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1982-11-30 under 510(k) number K823217. The device is classified under product code FKX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INPERSOL PERITONEAL DIALSIS CYCLER SET?

INPERSOL PERITONEAL DIALSIS CYCLER SET is a medical device that received FDA 510(k) clearance on 1982-11-30. The listed applicant is Abbott Laboratories. The 510(k) number is K823217.

When did INPERSOL PERITONEAL DIALSIS CYCLER SET receive FDA 510(k) clearance?

INPERSOL PERITONEAL DIALSIS CYCLER SET received FDA 510(k) clearance on 1982-11-30, under 510(k) number K823217.

Who is the listed applicant for INPERSOL PERITONEAL DIALSIS CYCLER SET?

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

What is the FDA product code for INPERSOL PERITONEAL DIALSIS CYCLER SET?

The FDA product code for INPERSOL PERITONEAL DIALSIS CYCLER SET is FKX.

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 Abbott Laboratories 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.

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Related Devices (Code: FKX)

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.

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