PRE-MOISTENED CLEANSING PAD
K-Number: K890514 · 1989-04-10
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Device Summary
Frequently Asked Questions
What is the PRE-MOISTENED CLEANSING PAD?
PRE-MOISTENED CLEANSING PAD is a medical device that received FDA 510(k) clearance on 1989-04-10. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K890514.
When did PRE-MOISTENED CLEANSING PAD receive FDA 510(k) clearance?
PRE-MOISTENED CLEANSING PAD received FDA 510(k) clearance on 1989-04-10, under 510(k) number K890514.
Who is the listed applicant for PRE-MOISTENED CLEANSING PAD?
The FDA 510(k) record lists Bausch & Lomb, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRE-MOISTENED CLEANSING PAD?
The FDA product code for PRE-MOISTENED CLEANSING PAD is LKB.
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 Bausch & Lomb, 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: LKB)
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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