PERITONEAL DIALYSIS SYSTEM AND ACCESS.
K-Number: K893712 · 1989-07-24
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Device Summary
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.
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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