MODEL A15-103
K-Number: K953192 · 1995-09-05
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Device Summary
Frequently Asked Questions
What is the MODEL A15-103?
MODEL A15-103 is a medical device that received FDA 510(k) clearance on 1995-09-05. The listed applicant is Beaverstate Dental, Inc.. The 510(k) number is K953192.
When did MODEL A15-103 receive FDA 510(k) clearance?
MODEL A15-103 received FDA 510(k) clearance on 1995-09-05, under 510(k) number K953192.
Who is the listed applicant for MODEL A15-103?
The FDA 510(k) record lists Beaverstate Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL A15-103?
The FDA product code for MODEL A15-103 is EAY.
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 Beaverstate Dental, 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: EAY)
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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