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FDA 510(k)

RUSCH ENDOTRACHEAL TUBE STYLET

K-Number: K952100 · 1995-08-08

ApplicantRusch, Inc.
Decision Date1995-08-08
Product CodeBSR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RUSCH ENDOTRACHEAL TUBE STYLET is the device name listed in this FDA 510(k) record. The listed applicant is Rusch, Inc.. It received FDA 510(k) clearance on 1995-08-08 under 510(k) number K952100. The device is classified under product code BSR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 26 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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