ADVANCED PERFORM HOLLOW FIBER DIALYZER, 019752-5
K-Number: K861537 · 1986-07-10
Advertisement
Device Summary
Frequently Asked Questions
What is the ADVANCED PERFORM HOLLOW FIBER DIALYZER, 019752-5?
ADVANCED PERFORM HOLLOW FIBER DIALYZER, 019752-5 is a medical device that received FDA 510(k) clearance on 1986-07-10. The listed applicant is National Medical Care, Medical Products Div., Inc.. The 510(k) number is K861537.
When did ADVANCED PERFORM HOLLOW FIBER DIALYZER, 019752-5 receive FDA 510(k) clearance?
ADVANCED PERFORM HOLLOW FIBER DIALYZER, 019752-5 received FDA 510(k) clearance on 1986-07-10, under 510(k) number K861537.
Who is the listed applicant for ADVANCED PERFORM HOLLOW FIBER DIALYZER, 019752-5?
The FDA 510(k) record lists National Medical Care, Medical Products Div., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADVANCED PERFORM HOLLOW FIBER DIALYZER, 019752-5?
The FDA product code for ADVANCED PERFORM HOLLOW FIBER DIALYZER, 019752-5 is FJI.
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 National Medical Care, Medical Products Div., 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: FJI)
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