BIOSCRUB SURGICAL SCRUB BRUSH
K-Number: K870258 · 1987-02-24
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Device Summary
Frequently Asked Questions
What is the BIOSCRUB SURGICAL SCRUB BRUSH?
BIOSCRUB SURGICAL SCRUB BRUSH is a medical device that received FDA 510(k) clearance on 1987-02-24. The listed applicant is K. W. Griffen Co.. The 510(k) number is K870258.
When did BIOSCRUB SURGICAL SCRUB BRUSH receive FDA 510(k) clearance?
BIOSCRUB SURGICAL SCRUB BRUSH received FDA 510(k) clearance on 1987-02-24, under 510(k) number K870258.
Who is the listed applicant for BIOSCRUB SURGICAL SCRUB BRUSH?
The FDA 510(k) record lists K. W. Griffen Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOSCRUB SURGICAL SCRUB BRUSH?
The FDA product code for BIOSCRUB SURGICAL SCRUB BRUSH is GEC.
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 K. W. Griffen Co. 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: GEC)
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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