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FDA 510(k)

RUSCH AGT PVC PREF ORAL TRACH TUBE, UNCUF W/MUR EY

K-Number: K931166 · 1993-06-22

ApplicantRusch, Inc.
Decision Date1993-06-22
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RUSCH AGT PVC PREF ORAL TRACH TUBE, UNCUF W/MUR EY is the device name listed in this FDA 510(k) record. The listed applicant is Rusch, Inc.. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K931166. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUSCH AGT PVC PREF ORAL TRACH TUBE, UNCUF W/MUR EY?

RUSCH AGT PVC PREF ORAL TRACH TUBE, UNCUF W/MUR EY is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Rusch, Inc.. The 510(k) number is K931166.

When did RUSCH AGT PVC PREF ORAL TRACH TUBE, UNCUF W/MUR EY receive FDA 510(k) clearance?

RUSCH AGT PVC PREF ORAL TRACH TUBE, UNCUF W/MUR EY received FDA 510(k) clearance on 1993-06-22, under 510(k) number K931166.

Who is the listed applicant for RUSCH AGT PVC PREF ORAL TRACH TUBE, UNCUF W/MUR EY?

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 AGT PVC PREF ORAL TRACH TUBE, UNCUF W/MUR EY?

The FDA product code for RUSCH AGT PVC PREF ORAL TRACH TUBE, UNCUF W/MUR EY is BTR.

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.

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Related Devices (Code: BTR)

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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