T.E.A.R. TECH3
K-Number: K090532 · 2009-11-13
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Device Summary
Frequently Asked Questions
What is the T.E.A.R. TECH3?
T.E.A.R. TECH3 is a medical device that received FDA 510(k) clearance on 2009-11-13. The listed applicant is Vision Quest Industries, Inc.. The 510(k) number is K090532.
When did T.E.A.R. TECH3 receive FDA 510(k) clearance?
T.E.A.R. TECH3 received FDA 510(k) clearance on 2009-11-13, under 510(k) number K090532.
Who is the listed applicant for T.E.A.R. TECH3?
The FDA 510(k) record lists Vision Quest Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T.E.A.R. TECH3?
The FDA product code for T.E.A.R. TECH3 is IPF.
Other records listing Vision Quest Industries, 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: IPF)
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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