STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM IN
K-Number: K850214 · 1985-07-26
Advertisement
Device Summary
Frequently Asked Questions
What is the STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM IN?
STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM IN is a medical device that received FDA 510(k) clearance on 1985-07-26. The listed applicant is Accurate Surgical Instruments Co.. The 510(k) number is K850214.
When did STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM IN receive FDA 510(k) clearance?
STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM IN received FDA 510(k) clearance on 1985-07-26, under 510(k) number K850214.
Who is the listed applicant for STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM IN?
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 STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM IN?
The FDA product code for STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM IN 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.
Advertisement