NEDBOND EJECTOR KERRISON RONGEUR
K-Number: K933978 · 1994-01-12
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Device Summary
Frequently Asked Questions
What is the NEDBOND EJECTOR KERRISON RONGEUR?
NEDBOND EJECTOR KERRISON RONGEUR is a medical device that received FDA 510(k) clearance on 1994-01-12. The listed applicant is Redmond Neurotechnologies Corp.. The 510(k) number is K933978.
When did NEDBOND EJECTOR KERRISON RONGEUR receive FDA 510(k) clearance?
NEDBOND EJECTOR KERRISON RONGEUR received FDA 510(k) clearance on 1994-01-12, under 510(k) number K933978.
Who is the listed applicant for NEDBOND EJECTOR KERRISON RONGEUR?
The FDA 510(k) record lists Redmond Neurotechnologies Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEDBOND EJECTOR KERRISON RONGEUR?
The FDA product code for NEDBOND EJECTOR KERRISON RONGEUR is HAE.
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: HAE)
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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