HEMODIALYSIS TRANSDUCER PROTECTOR
K-Number: K812162 · 1981-09-24
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Device Summary
Frequently Asked Questions
What is the HEMODIALYSIS TRANSDUCER PROTECTOR?
HEMODIALYSIS TRANSDUCER PROTECTOR is a medical device that received FDA 510(k) clearance on 1981-09-24. The listed applicant is Membrana. The 510(k) number is K812162.
When did HEMODIALYSIS TRANSDUCER PROTECTOR receive FDA 510(k) clearance?
HEMODIALYSIS TRANSDUCER PROTECTOR received FDA 510(k) clearance on 1981-09-24, under 510(k) number K812162.
Who is the listed applicant for HEMODIALYSIS TRANSDUCER PROTECTOR?
The FDA 510(k) record lists Membrana as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMODIALYSIS TRANSDUCER PROTECTOR?
The FDA product code for HEMODIALYSIS TRANSDUCER PROTECTOR is FIB.
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.
Related Devices (Code: FIB)
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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