STYLET AND TRACHEAL LIGHTWAND (STL)
K-Number: K922842 · 1992-12-18
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Device Summary
Frequently Asked Questions
What is the STYLET AND TRACHEAL LIGHTWAND (STL)?
STYLET AND TRACHEAL LIGHTWAND (STL) is a medical device that received FDA 510(k) clearance on 1992-12-18. The listed applicant is Laerdal California, Inc.. The 510(k) number is K922842.
When did STYLET AND TRACHEAL LIGHTWAND (STL) receive FDA 510(k) clearance?
STYLET AND TRACHEAL LIGHTWAND (STL) received FDA 510(k) clearance on 1992-12-18, under 510(k) number K922842.
Who is the listed applicant for STYLET AND TRACHEAL LIGHTWAND (STL)?
The FDA 510(k) record lists Laerdal California, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STYLET AND TRACHEAL LIGHTWAND (STL)?
The FDA product code for STYLET AND TRACHEAL LIGHTWAND (STL) 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 Laerdal California, 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: 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.
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