SWAN-NECK PERITONEAL DIALYSIS CATHETERS
K-Number: K862046 · 1986-06-19
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Device Summary
Frequently Asked Questions
What is the SWAN-NECK PERITONEAL DIALYSIS CATHETERS?
SWAN-NECK PERITONEAL DIALYSIS CATHETERS is a medical device that received FDA 510(k) clearance on 1986-06-19. The listed applicant is Accurate Surgical Instruments Co.. The 510(k) number is K862046.
When did SWAN-NECK PERITONEAL DIALYSIS CATHETERS receive FDA 510(k) clearance?
SWAN-NECK PERITONEAL DIALYSIS CATHETERS received FDA 510(k) clearance on 1986-06-19, under 510(k) number K862046.
Who is the listed applicant for SWAN-NECK PERITONEAL DIALYSIS CATHETERS?
The FDA 510(k) record lists Accurate Surgical Instruments Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SWAN-NECK PERITONEAL DIALYSIS CATHETERS?
The FDA product code for SWAN-NECK PERITONEAL DIALYSIS CATHETERS 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 Accurate Surgical Instruments Co. 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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