DEXTROLYTE II PERITONEAL DIALYSIS ADMIN. SET
K-Number: K920586 · 1992-09-21
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Device Summary
Frequently Asked Questions
What is the DEXTROLYTE II PERITONEAL DIALYSIS ADMIN. SET?
DEXTROLYTE II PERITONEAL DIALYSIS ADMIN. SET is a medical device that received FDA 510(k) clearance on 1992-09-21. The listed applicant is National Medical Care, Medical Products Div., Inc.. The 510(k) number is K920586.
When did DEXTROLYTE II PERITONEAL DIALYSIS ADMIN. SET receive FDA 510(k) clearance?
DEXTROLYTE II PERITONEAL DIALYSIS ADMIN. SET received FDA 510(k) clearance on 1992-09-21, under 510(k) number K920586.
Who is the listed applicant for DEXTROLYTE II PERITONEAL DIALYSIS ADMIN. SET?
The FDA 510(k) record lists National Medical Care, Medical Products Div., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEXTROLYTE II PERITONEAL DIALYSIS ADMIN. SET?
The FDA product code for DEXTROLYTE II PERITONEAL DIALYSIS ADMIN. SET 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 National Medical Care, Medical Products Div., 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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