TRITON HUDSON CHUCK ATTACHMENT
K-Number: K983092 · 1998-11-06
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Device Summary
Frequently Asked Questions
What is the TRITON HUDSON CHUCK ATTACHMENT?
TRITON HUDSON CHUCK ATTACHMENT is a medical device that received FDA 510(k) clearance on 1998-11-06. The listed applicant is Mednext, Inc.. The 510(k) number is K983092.
When did TRITON HUDSON CHUCK ATTACHMENT receive FDA 510(k) clearance?
TRITON HUDSON CHUCK ATTACHMENT received FDA 510(k) clearance on 1998-11-06, under 510(k) number K983092.
Who is the listed applicant for TRITON HUDSON CHUCK ATTACHMENT?
The FDA 510(k) record lists Mednext, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRITON HUDSON CHUCK ATTACHMENT?
The FDA product code for TRITON HUDSON CHUCK ATTACHMENT is HBB.
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 Mednext, 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: HBB)
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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