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FDA 510(k)

PERITONEAL DIALYSIS DRAINAGE

K-Number: K812771 · 1981-10-19

Decision Date1981-10-19
Product CodeKDJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PERITONEAL DIALYSIS DRAINAGE is the device name listed in this FDA 510(k) record. The listed applicant is Dravon Medical, Inc.. It received FDA 510(k) clearance on 1981-10-19 under 510(k) number K812771. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERITONEAL DIALYSIS DRAINAGE?

PERITONEAL DIALYSIS DRAINAGE is a medical device that received FDA 510(k) clearance on 1981-10-19. The listed applicant is Dravon Medical, Inc.. The 510(k) number is K812771.

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

PERITONEAL DIALYSIS DRAINAGE received FDA 510(k) clearance on 1981-10-19, under 510(k) number K812771.

Who is the listed applicant for PERITONEAL DIALYSIS DRAINAGE?

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

What is the FDA product code for PERITONEAL DIALYSIS DRAINAGE?

The FDA product code for PERITONEAL DIALYSIS DRAINAGE is KDJ.

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 Dravon Medical, 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 16 devices →

Related Devices (Code: KDJ)

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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