NEPHROSTOMY CONNECTING TUBE (A-50)
K-Number: K862581 · 1986-09-23
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Device Summary
Frequently Asked Questions
What is the NEPHROSTOMY CONNECTING TUBE (A-50)?
NEPHROSTOMY CONNECTING TUBE (A-50) is a medical device that received FDA 510(k) clearance on 1986-09-23. The listed applicant is Advanced Clinical Products, Inc.. The 510(k) number is K862581.
When did NEPHROSTOMY CONNECTING TUBE (A-50) receive FDA 510(k) clearance?
NEPHROSTOMY CONNECTING TUBE (A-50) received FDA 510(k) clearance on 1986-09-23, under 510(k) number K862581.
Who is the listed applicant for NEPHROSTOMY CONNECTING TUBE (A-50)?
The FDA 510(k) record lists Advanced Clinical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEPHROSTOMY CONNECTING TUBE (A-50)?
The FDA product code for NEPHROSTOMY CONNECTING TUBE (A-50) is KNX.
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 Advanced Clinical Products, 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: KNX)
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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