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FDA 510(k)

DENTURE ADHESIVE SEALS

K-Number: K831493 · 1983-06-30

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1983-06-30
Product CodeKOT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTURE ADHESIVE SEALS is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1983-06-30 under 510(k) number K831493. The device is classified under product code KOT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTURE ADHESIVE SEALS?

DENTURE ADHESIVE SEALS is a medical device that received FDA 510(k) clearance on 1983-06-30. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K831493.

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

DENTURE ADHESIVE SEALS received FDA 510(k) clearance on 1983-06-30, under 510(k) number K831493.

Who is the listed applicant for DENTURE ADHESIVE SEALS?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTURE ADHESIVE SEALS?

The FDA product code for DENTURE ADHESIVE SEALS is KOT.

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Other records listing Johnson & Johnson Professionals, Inc. as applicant

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Related Devices (Code: KOT)

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.

K945462SUPER POLI-GRIP DENTURE ADHESIVE CREAMBlock Drug Company, Inc.K941365MPI DENTURE ADHESIVE FILM SEALSMedical Polymers, Inc.K903568SUPER STRENGTH DENTURE ADHESIVE CREAMTeledyne GetzK895818STEADFAST DENTURE ADHESIVE CREAMStiefel Research Institute, Inc.K884357PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEMPrecision Dynamics Corp.K872225SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDERBlock Drug Company, Inc.

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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