QUIK-BRUSH
K-Number: K870414 · 1987-06-11
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Device Summary
Frequently Asked Questions
What is the QUIK-BRUSH?
QUIK-BRUSH is a medical device that received FDA 510(k) clearance on 1987-06-11. The listed applicant is Intl. Medication Systems, Ltd.. The 510(k) number is K870414.
When did QUIK-BRUSH receive FDA 510(k) clearance?
QUIK-BRUSH received FDA 510(k) clearance on 1987-06-11, under 510(k) number K870414.
Who is the listed applicant for QUIK-BRUSH?
The FDA 510(k) record lists Intl. Medication Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUIK-BRUSH?
The FDA product code for QUIK-BRUSH is EFW.
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 Intl. Medication Systems, Ltd. 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: EFW)
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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