STERI-CLENS WOUND CARE KIT
K-Number: K883250 · 1988-08-26
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Device Summary
Frequently Asked Questions
What is the STERI-CLENS WOUND CARE KIT?
STERI-CLENS WOUND CARE KIT is a medical device that received FDA 510(k) clearance on 1988-08-26. The listed applicant is Absorbent Cotton Co., Inc.. The 510(k) number is K883250.
When did STERI-CLENS WOUND CARE KIT receive FDA 510(k) clearance?
STERI-CLENS WOUND CARE KIT received FDA 510(k) clearance on 1988-08-26, under 510(k) number K883250.
Who is the listed applicant for STERI-CLENS WOUND CARE KIT?
The FDA 510(k) record lists Absorbent Cotton Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERI-CLENS WOUND CARE KIT?
The FDA product code for STERI-CLENS WOUND CARE KIT is LRO.
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 Absorbent Cotton Co., Inc. 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: LRO)
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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