HODGE DECOMPRESSION TUBE
K-Number: K834258 · 1984-02-04
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Device Summary
Frequently Asked Questions
What is the HODGE DECOMPRESSION TUBE?
HODGE DECOMPRESSION TUBE is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Inmed Corp.. The 510(k) number is K834258.
When did HODGE DECOMPRESSION TUBE receive FDA 510(k) clearance?
HODGE DECOMPRESSION TUBE received FDA 510(k) clearance on 1984-02-04, under 510(k) number K834258.
Who is the listed applicant for HODGE DECOMPRESSION TUBE?
The FDA 510(k) record lists Inmed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HODGE DECOMPRESSION TUBE?
The FDA product code for HODGE DECOMPRESSION TUBE is KNT.
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 Inmed Corp. 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: KNT)
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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