RUSCH ENDOTRACHEAL TUBE STYLET
K-Number: K952100 · 1995-08-08
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Device Summary
Frequently Asked Questions
What is the RUSCH ENDOTRACHEAL TUBE STYLET?
RUSCH ENDOTRACHEAL TUBE STYLET is a medical device that received FDA 510(k) clearance on 1995-08-08. The listed applicant is Rusch, Inc.. The 510(k) number is K952100.
When did RUSCH ENDOTRACHEAL TUBE STYLET receive FDA 510(k) clearance?
RUSCH ENDOTRACHEAL TUBE STYLET received FDA 510(k) clearance on 1995-08-08, under 510(k) number K952100.
Who is the listed applicant for RUSCH ENDOTRACHEAL TUBE STYLET?
The FDA 510(k) record lists Rusch, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RUSCH ENDOTRACHEAL TUBE STYLET?
The FDA product code for RUSCH ENDOTRACHEAL TUBE STYLET is BSR.
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 Rusch, 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: BSR)
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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