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FDA 510(k)

SEA-BOND ADHEVISE DENTURE CUSHIONS

K-Number: K770175 · 1977-02-04

ApplicantCombe, Inc.
Decision Date1977-02-04
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SEA-BOND ADHEVISE DENTURE CUSHIONS is the device name listed in this FDA 510(k) record. The listed applicant is Combe, Inc.. It received FDA 510(k) clearance on 1977-02-04 under 510(k) number K770175. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEA-BOND ADHEVISE DENTURE CUSHIONS?

SEA-BOND ADHEVISE DENTURE CUSHIONS is a medical device that received FDA 510(k) clearance on 1977-02-04. The listed applicant is Combe, Inc.. The 510(k) number is K770175.

When did SEA-BOND ADHEVISE DENTURE CUSHIONS receive FDA 510(k) clearance?

SEA-BOND ADHEVISE DENTURE CUSHIONS received FDA 510(k) clearance on 1977-02-04, under 510(k) number K770175.

Who is the listed applicant for SEA-BOND ADHEVISE DENTURE CUSHIONS?

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

What is the FDA product code for SEA-BOND ADHEVISE DENTURE CUSHIONS?

The FDA product code for SEA-BOND ADHEVISE DENTURE CUSHIONS is KKX.

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.

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Other records listing Combe, 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.

K942203OTC DENTURE CLEANSERK925259CFR MONOGRAPHK863375SEA-BONDK780719FUNGUS FIGHTER INSOLESK770413CUSHIONS, DENTURE ADHESIVE, ALL-DAY

Related Devices (Code: KKX)

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.

K230645BeneHold™ Surgical Incise Drape with CHG antimicrobial IIAvery Dennison Medical , Ltd.K2225783M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)3M CompanyK202208BeneHold Surgical Incise Drape with CHG antimicrobialAvery Dennison Belgie BvbaK200238ControlRad Sterile CoverControlrad, Inc.K163556MediClear PreOpCovalontechnologies, Inc.K130404TIBURON SURGICAL DRAPECardinal Health200, LLC

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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