XOMED-TREACE SCOPESHEATH
K-Number: K933672 · 1994-07-18
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Device Summary
Frequently Asked Questions
What is the XOMED-TREACE SCOPESHEATH?
XOMED-TREACE SCOPESHEATH is a medical device that received FDA 510(k) clearance on 1994-07-18. The listed applicant is Xomed-Treace, Inc.. The 510(k) number is K933672.
When did XOMED-TREACE SCOPESHEATH receive FDA 510(k) clearance?
XOMED-TREACE SCOPESHEATH received FDA 510(k) clearance on 1994-07-18, under 510(k) number K933672.
Who is the listed applicant for XOMED-TREACE SCOPESHEATH?
The FDA 510(k) record lists Xomed-Treace, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XOMED-TREACE SCOPESHEATH?
The FDA product code for XOMED-TREACE SCOPESHEATH is EOB.
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 Xomed-Treace, 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: EOB)
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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