ARRIRM SCRUB BRUSH/SPONGE
K-Number: K823173 · 1982-11-22
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Device Summary
Frequently Asked Questions
What is the ARRIRM SCRUB BRUSH/SPONGE?
ARRIRM SCRUB BRUSH/SPONGE is a medical device that received FDA 510(k) clearance on 1982-11-22. The listed applicant is The Buckeye Cellulose Corp.. The 510(k) number is K823173.
When did ARRIRM SCRUB BRUSH/SPONGE receive FDA 510(k) clearance?
ARRIRM SCRUB BRUSH/SPONGE received FDA 510(k) clearance on 1982-11-22, under 510(k) number K823173.
Who is the listed applicant for ARRIRM SCRUB BRUSH/SPONGE?
The FDA 510(k) record lists The Buckeye Cellulose Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARRIRM SCRUB BRUSH/SPONGE?
The FDA product code for ARRIRM SCRUB BRUSH/SPONGE 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 The Buckeye Cellulose Corp. 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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