DISPOSABLE SCREW TYPE PROPHY BRUSH
K-Number: K900507 · 1990-04-10
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE SCREW TYPE PROPHY BRUSH?
DISPOSABLE SCREW TYPE PROPHY BRUSH is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Dentsply Intl.. The 510(k) number is K900507.
When did DISPOSABLE SCREW TYPE PROPHY BRUSH receive FDA 510(k) clearance?
DISPOSABLE SCREW TYPE PROPHY BRUSH received FDA 510(k) clearance on 1990-04-10, under 510(k) number K900507.
Who is the listed applicant for DISPOSABLE SCREW TYPE PROPHY BRUSH?
The FDA 510(k) record lists Dentsply Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE SCREW TYPE PROPHY BRUSH?
The FDA product code for DISPOSABLE SCREW TYPE PROPHY BRUSH is EHK.
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 Intl. 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: EHK)
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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