VETA PERITONEAL DIALYSIS CATHETER
K-Number: K113354 · 2012-03-13
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Device Summary
Frequently Asked Questions
What is the VETA PERITONEAL DIALYSIS CATHETER?
VETA PERITONEAL DIALYSIS CATHETER is a medical device that received FDA 510(k) clearance on 2012-03-13. The listed applicant is Pfm Medical, Inc.. The 510(k) number is K113354.
When did VETA PERITONEAL DIALYSIS CATHETER receive FDA 510(k) clearance?
VETA PERITONEAL DIALYSIS CATHETER received FDA 510(k) clearance on 2012-03-13, under 510(k) number K113354.
Who is the listed applicant for VETA PERITONEAL DIALYSIS CATHETER?
The FDA 510(k) record lists Pfm Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VETA PERITONEAL DIALYSIS CATHETER?
The FDA product code for VETA PERITONEAL DIALYSIS CATHETER is FJS.
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 Pfm 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.
Related Devices (Code: FJS)
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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