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FDA 510(k)

PERIDIAL PERITONEAL DIALYSIS TRAY

K-Number: K792207 · 1979-12-10

Decision Date1979-12-10
Product CodeFKG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PERIDIAL PERITONEAL DIALYSIS TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1979-12-10 under 510(k) number K792207. The device is classified under product code FKG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIDIAL PERITONEAL DIALYSIS TRAY?

PERIDIAL PERITONEAL DIALYSIS TRAY is a medical device that received FDA 510(k) clearance on 1979-12-10. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K792207.

When did PERIDIAL PERITONEAL DIALYSIS TRAY receive FDA 510(k) clearance?

PERIDIAL PERITONEAL DIALYSIS TRAY received FDA 510(k) clearance on 1979-12-10, under 510(k) number K792207.

Who is the listed applicant for PERIDIAL PERITONEAL DIALYSIS TRAY?

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

What is the FDA product code for PERIDIAL PERITONEAL DIALYSIS TRAY?

The FDA product code for PERIDIAL PERITONEAL DIALYSIS TRAY is FKG.

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 Cutter Laboratories, 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: FKG)

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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