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FDA 510(k)

PEPSODENT DENTURE ADHESIVE CREAM

K-Number: K850610 · 1985-05-15

ApplicantLever Brothers Company, Inc.
Decision Date1985-05-15
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PEPSODENT DENTURE ADHESIVE CREAM is the device name listed in this FDA 510(k) record. The listed applicant is Lever Brothers Company, Inc.. It received FDA 510(k) clearance on 1985-05-15 under 510(k) number K850610. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEPSODENT DENTURE ADHESIVE CREAM?

PEPSODENT DENTURE ADHESIVE CREAM is a medical device that received FDA 510(k) clearance on 1985-05-15. The listed applicant is Lever Brothers Company, Inc.. The 510(k) number is K850610.

When did PEPSODENT DENTURE ADHESIVE CREAM receive FDA 510(k) clearance?

PEPSODENT DENTURE ADHESIVE CREAM received FDA 510(k) clearance on 1985-05-15, under 510(k) number K850610.

Who is the listed applicant for PEPSODENT DENTURE ADHESIVE CREAM?

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 ADHESIVE CREAM?

The FDA product code for PEPSODENT DENTURE ADHESIVE CREAM is EBD.

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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.

K851182PEPSODENT DENTURE CLEANSER-WESTONE FORMULAK851183PEPSODENT DENTURE CLEANSER PDP FORMULAK781018DX TOOTHBRUSH

Related Devices (Code: EBD)

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.

K254091GLOSSY COAT (15ML)YAMAHACHI DENTAL MFG., Co.K250804ID LIGHT CURE SYSTEMId Korea Co., Ltd.K240735visio.lign color, visio.lign shieldBredent GmbH & Co. KGK223365RODIN Palette Naturalizing KitBelport Company, Inc., Gingi-PakK211854VITA Akzent LCVita Zahnfabrik GmbH H Rauter & COK162408Nano Varnish, Plaquit, Lightpaint on SurfaceDreve Dentamid GmbH

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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