Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE

K-Number: K955238 · 1996-02-06

ApplicantRusch Intl.
Decision Date1996-02-06
Product CodeBSR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE is the device name listed in this FDA 510(k) record. The listed applicant is Rusch Intl.. It received FDA 510(k) clearance on 1996-02-06 under 510(k) number K955238. 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 SCHROEDER ENDOTRACHEAL TUBE STYLE?

RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE is a medical device that received FDA 510(k) clearance on 1996-02-06. The listed applicant is Rusch Intl.. The 510(k) number is K955238.

When did RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE receive FDA 510(k) clearance?

RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE received FDA 510(k) clearance on 1996-02-06, under 510(k) number K955238.

Who is the listed applicant for RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE?

The FDA 510(k) record lists Rusch Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE?

The FDA product code for RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE 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 Intl. 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 43 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

View on FDA Database →

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

↑