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FDA 510(k)

PERITONEAL DIALYSIS SYSTEM AND ACCESS.

K-Number: K893712 · 1989-07-24

ApplicantDelmed, Inc.
Decision Date1989-07-24
Product CodeKDJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PERITONEAL DIALYSIS SYSTEM AND ACCESS. is the device name listed in this FDA 510(k) record. The listed applicant is Delmed, Inc.. It received FDA 510(k) clearance on 1989-07-24 under 510(k) number K893712. 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 SYSTEM AND ACCESS.?

PERITONEAL DIALYSIS SYSTEM AND ACCESS. is a medical device that received FDA 510(k) clearance on 1989-07-24. The listed applicant is Delmed, Inc.. The 510(k) number is K893712.

When did PERITONEAL DIALYSIS SYSTEM AND ACCESS. receive FDA 510(k) clearance?

PERITONEAL DIALYSIS SYSTEM AND ACCESS. received FDA 510(k) clearance on 1989-07-24, under 510(k) number K893712.

Who is the listed applicant for PERITONEAL DIALYSIS SYSTEM AND ACCESS.?

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

What is the FDA product code for PERITONEAL DIALYSIS SYSTEM AND ACCESS.?

The FDA product code for PERITONEAL DIALYSIS SYSTEM AND ACCESS. 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 Delmed, 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 27 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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