MODIFICATION IN MEMBRANE HOUSING CONFI
K-Number: K832925 · 1983-11-28
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Device Summary
Frequently Asked Questions
What is the MODIFICATION IN MEMBRANE HOUSING CONFI?
MODIFICATION IN MEMBRANE HOUSING CONFI is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Ries Biologicals. The 510(k) number is K832925.
When did MODIFICATION IN MEMBRANE HOUSING CONFI receive FDA 510(k) clearance?
MODIFICATION IN MEMBRANE HOUSING CONFI received FDA 510(k) clearance on 1983-11-28, under 510(k) number K832925.
Who is the listed applicant for MODIFICATION IN MEMBRANE HOUSING CONFI?
The FDA 510(k) record lists Ries Biologicals as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION IN MEMBRANE HOUSING CONFI?
The FDA product code for MODIFICATION IN MEMBRANE HOUSING CONFI is KOC.
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 Ries Biologicals 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: KOC)
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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