PEPSODENT DENTURE CLEANSER-WESTONE FORMULA
K-Number: K851182 · 1985-04-29
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Device Summary
Frequently Asked Questions
What is the PEPSODENT DENTURE CLEANSER-WESTONE FORMULA?
PEPSODENT DENTURE CLEANSER-WESTONE FORMULA is a medical device that received FDA 510(k) clearance on 1985-04-29. The listed applicant is Lever Brothers Company, Inc.. The 510(k) number is K851182.
When did PEPSODENT DENTURE CLEANSER-WESTONE FORMULA receive FDA 510(k) clearance?
PEPSODENT DENTURE CLEANSER-WESTONE FORMULA received FDA 510(k) clearance on 1985-04-29, under 510(k) number K851182.
Who is the listed applicant for PEPSODENT DENTURE CLEANSER-WESTONE FORMULA?
The FDA 510(k) record lists Lever Brothers Company, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PEPSODENT DENTURE CLEANSER-WESTONE FORMULA?
The FDA product code for PEPSODENT DENTURE CLEANSER-WESTONE FORMULA is EFT.
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 Lever Brothers Company, 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: EFT)
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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