HOLDE.T. ENDOTRACHEAL TUBE STABILIZATION BAR
K-Number: K934288 · 1994-06-09
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Device Summary
Frequently Asked Questions
What is the HOLDE.T. ENDOTRACHEAL TUBE STABILIZATION BAR?
HOLDE.T. ENDOTRACHEAL TUBE STABILIZATION BAR is a medical device that received FDA 510(k) clearance on 1994-06-09. The listed applicant is Neo-Tech, Inc.. The 510(k) number is K934288.
When did HOLDE.T. ENDOTRACHEAL TUBE STABILIZATION BAR receive FDA 510(k) clearance?
HOLDE.T. ENDOTRACHEAL TUBE STABILIZATION BAR received FDA 510(k) clearance on 1994-06-09, under 510(k) number K934288.
Who is the listed applicant for HOLDE.T. ENDOTRACHEAL TUBE STABILIZATION BAR?
The FDA 510(k) record lists Neo-Tech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HOLDE.T. ENDOTRACHEAL TUBE STABILIZATION BAR?
The FDA product code for HOLDE.T. ENDOTRACHEAL TUBE STABILIZATION BAR is CBH.
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: CBH)
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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