TIGER ENDOTRACHEAL TUBES (VARIOUS MODELS AND SIZES)
K-Number: K041311 · 2005-03-18
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Device Summary
Frequently Asked Questions
What is the TIGER ENDOTRACHEAL TUBES (VARIOUS MODELS AND SIZES)?
TIGER ENDOTRACHEAL TUBES (VARIOUS MODELS AND SIZES) is a medical device that received FDA 510(k) clearance on 2005-03-18. The listed applicant is Tiger Medical Products, Ltd.. The 510(k) number is K041311.
When did TIGER ENDOTRACHEAL TUBES (VARIOUS MODELS AND SIZES) receive FDA 510(k) clearance?
TIGER ENDOTRACHEAL TUBES (VARIOUS MODELS AND SIZES) received FDA 510(k) clearance on 2005-03-18, under 510(k) number K041311.
Who is the listed applicant for TIGER ENDOTRACHEAL TUBES (VARIOUS MODELS AND SIZES)?
The FDA 510(k) record lists Tiger Medical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TIGER ENDOTRACHEAL TUBES (VARIOUS MODELS AND SIZES)?
The FDA product code for TIGER ENDOTRACHEAL TUBES (VARIOUS MODELS AND SIZES) 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 Tiger Medical Products, Ltd. 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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