CURITY SURGICAL SCRUB BRUSH SPONGE
K-Number: K820086 · 1982-01-28
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Device Summary
Frequently Asked Questions
What is the CURITY SURGICAL SCRUB BRUSH SPONGE?
CURITY SURGICAL SCRUB BRUSH SPONGE is a medical device that received FDA 510(k) clearance on 1982-01-28. The listed applicant is The Kendal Co.. The 510(k) number is K820086.
When did CURITY SURGICAL SCRUB BRUSH SPONGE receive FDA 510(k) clearance?
CURITY SURGICAL SCRUB BRUSH SPONGE received FDA 510(k) clearance on 1982-01-28, under 510(k) number K820086.
Who is the listed applicant for CURITY SURGICAL SCRUB BRUSH SPONGE?
The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CURITY SURGICAL SCRUB BRUSH SPONGE?
The FDA product code for CURITY SURGICAL 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 Kendal 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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