PERITONEAL DIALYSIS COIL CATHETER
K-Number: K850247 · 1985-02-14
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Device Summary
Frequently Asked Questions
What is the PERITONEAL DIALYSIS COIL CATHETER?
PERITONEAL DIALYSIS COIL CATHETER is a medical device that received FDA 510(k) clearance on 1985-02-14. The listed applicant is Sil-Med Corp.. The 510(k) number is K850247.
When did PERITONEAL DIALYSIS COIL CATHETER receive FDA 510(k) clearance?
PERITONEAL DIALYSIS COIL CATHETER received FDA 510(k) clearance on 1985-02-14, under 510(k) number K850247.
Who is the listed applicant for PERITONEAL DIALYSIS COIL CATHETER?
The FDA 510(k) record lists Sil-Med Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERITONEAL DIALYSIS COIL CATHETER?
The FDA product code for PERITONEAL DIALYSIS COIL CATHETER is FXX.
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 Sil-Med Corp. 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: FXX)
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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