RUSCH AGT PVC PREFORM ORAL TRACH TUB/CUF W/MUR EYE
K-Number: K931163 · 1993-06-23
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Device Summary
Frequently Asked Questions
What is the RUSCH AGT PVC PREFORM ORAL TRACH TUB/CUF W/MUR EYE?
RUSCH AGT PVC PREFORM ORAL TRACH TUB/CUF W/MUR EYE is a medical device that received FDA 510(k) clearance on 1993-06-23. The listed applicant is Rusch, Inc.. The 510(k) number is K931163.
When did RUSCH AGT PVC PREFORM ORAL TRACH TUB/CUF W/MUR EYE receive FDA 510(k) clearance?
RUSCH AGT PVC PREFORM ORAL TRACH TUB/CUF W/MUR EYE received FDA 510(k) clearance on 1993-06-23, under 510(k) number K931163.
Who is the listed applicant for RUSCH AGT PVC PREFORM ORAL TRACH TUB/CUF W/MUR EYE?
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 PREFORM ORAL TRACH TUB/CUF W/MUR EYE?
The FDA product code for RUSCH AGT PVC PREFORM ORAL TRACH TUB/CUF W/MUR EYE 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.
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
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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