BRACKET, METAL, ORTHODOTNIC
K-Number: K902809 · 1990-12-07
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Device Summary
Frequently Asked Questions
What is the BRACKET, METAL, ORTHODOTNIC?
BRACKET, METAL, ORTHODOTNIC is a medical device that received FDA 510(k) clearance on 1990-12-07. The listed applicant is Masel Industries, Inc.. The 510(k) number is K902809.
When did BRACKET, METAL, ORTHODOTNIC receive FDA 510(k) clearance?
BRACKET, METAL, ORTHODOTNIC received FDA 510(k) clearance on 1990-12-07, under 510(k) number K902809.
Who is the listed applicant for BRACKET, METAL, ORTHODOTNIC?
The FDA 510(k) record lists Masel Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRACKET, METAL, ORTHODOTNIC?
The FDA product code for BRACKET, METAL, ORTHODOTNIC is EJF.
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 Masel 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: EJF)
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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