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FDA 510(k)

BENT NECK CURLCATH PERITONEAL DIALYSIS KIT

K-Number: K874632 · 1987-12-29

ApplicantQuinton, Inc.
Decision Date1987-12-29
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BENT NECK CURLCATH PERITONEAL DIALYSIS KIT is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K874632. 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 BENT NECK CURLCATH PERITONEAL DIALYSIS KIT?

BENT NECK CURLCATH PERITONEAL DIALYSIS KIT is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Quinton, Inc.. The 510(k) number is K874632.

When did BENT NECK CURLCATH PERITONEAL DIALYSIS KIT receive FDA 510(k) clearance?

BENT NECK CURLCATH PERITONEAL DIALYSIS KIT received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874632.

Who is the listed applicant for BENT NECK CURLCATH PERITONEAL DIALYSIS KIT?

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

What is the FDA product code for BENT NECK CURLCATH PERITONEAL DIALYSIS KIT?

The FDA product code for BENT NECK CURLCATH PERITONEAL DIALYSIS KIT 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 Quinton, 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.

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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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