TAYLOR MADE MOBILE STANDER
K-Number: K922107 · 1992-05-26
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Device Summary
Frequently Asked Questions
What is the TAYLOR MADE MOBILE STANDER?
TAYLOR MADE MOBILE STANDER is a medical device that received FDA 510(k) clearance on 1992-05-26. The listed applicant is Nelson A. Taylor Co., Inc.. The 510(k) number is K922107.
When did TAYLOR MADE MOBILE STANDER receive FDA 510(k) clearance?
TAYLOR MADE MOBILE STANDER received FDA 510(k) clearance on 1992-05-26, under 510(k) number K922107.
Who is the listed applicant for TAYLOR MADE MOBILE STANDER?
The FDA 510(k) record lists Nelson A. Taylor Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAYLOR MADE MOBILE STANDER?
The FDA product code for TAYLOR MADE MOBILE STANDER is IPL.
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.
Related Devices (Code: IPL)
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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