THERMOFORM SHEET MATERIALS AND ACCESSORIES
K-Number: K072522 · 2007-11-16
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Device Summary
Frequently Asked Questions
What is the THERMOFORM SHEET MATERIALS AND ACCESSORIES?
THERMOFORM SHEET MATERIALS AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2007-11-16. The listed applicant is Dentsply International, Inc.. The 510(k) number is K072522.
When did THERMOFORM SHEET MATERIALS AND ACCESSORIES receive FDA 510(k) clearance?
THERMOFORM SHEET MATERIALS AND ACCESSORIES received FDA 510(k) clearance on 2007-11-16, under 510(k) number K072522.
Who is the listed applicant for THERMOFORM SHEET MATERIALS AND ACCESSORIES?
The FDA 510(k) record lists Dentsply International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THERMOFORM SHEET MATERIALS AND ACCESSORIES?
The FDA product code for THERMOFORM SHEET MATERIALS AND ACCESSORIES is MQC.
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 Dentsply International, 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: MQC)
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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