GAMBRO PERITONEAL DIALYSIS FLUID LINES
K-Number: K811294 · 1981-06-12
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Device Summary
Frequently Asked Questions
What is the GAMBRO PERITONEAL DIALYSIS FLUID LINES?
GAMBRO PERITONEAL DIALYSIS FLUID LINES is a medical device that received FDA 510(k) clearance on 1981-06-12. The listed applicant is Gambro, Inc.. The 510(k) number is K811294.
When did GAMBRO PERITONEAL DIALYSIS FLUID LINES receive FDA 510(k) clearance?
GAMBRO PERITONEAL DIALYSIS FLUID LINES received FDA 510(k) clearance on 1981-06-12, under 510(k) number K811294.
Who is the listed applicant for GAMBRO PERITONEAL DIALYSIS FLUID LINES?
The FDA 510(k) record lists Gambro, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GAMBRO PERITONEAL DIALYSIS FLUID LINES?
The FDA product code for GAMBRO PERITONEAL DIALYSIS FLUID LINES 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 Gambro, 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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