DOODLE BRUSH
K-Number: K800948 · 1980-05-08
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Device Summary
Frequently Asked Questions
What is the DOODLE BRUSH?
DOODLE BRUSH is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Lawton Surgical Instruments. The 510(k) number is K800948.
When did DOODLE BRUSH receive FDA 510(k) clearance?
DOODLE BRUSH received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800948.
Who is the listed applicant for DOODLE BRUSH?
The FDA 510(k) record lists Lawton Surgical Instruments as the applicant. This does not by itself establish the device manufacturer.
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 Lawton Surgical Instruments 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.
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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