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FDA 510(k)

BONDING AGENT, VYTOL

K-Number: K760400 · 1976-08-23

ApplicantL.D. Caulk Co.
Decision Date1976-08-23
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BONDING AGENT, VYTOL is the device name listed in this FDA 510(k) record. The listed applicant is L.D. Caulk Co.. It received FDA 510(k) clearance on 1976-08-23 under 510(k) number K760400. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONDING AGENT, VYTOL?

BONDING AGENT, VYTOL is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is L.D. Caulk Co.. The 510(k) number is K760400.

When did BONDING AGENT, VYTOL receive FDA 510(k) clearance?

BONDING AGENT, VYTOL received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760400.

Who is the listed applicant for BONDING AGENT, VYTOL?

The FDA 510(k) record lists L.D. Caulk Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BONDING AGENT, VYTOL?

The FDA product code for BONDING AGENT, VYTOL is KLE.

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Other records listing L.D. Caulk Co. 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.

K802262COMPOSITE RESTORATIVEK801690VALIANTK790586CHEMBONDK790585FINESSEK780560DENTAL AMALGAMATORK780384IMPROVED DYCAL

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Related Devices (Code: KLE)

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.

K262252MPa Max adhesiveDen-Mat Holdings, LLCK260485Any-EtchMediclus Co., Ltd.K260430Porcelain Etch GelBelport Company, Inc., Gingi-PakK252450Adhese 2Ivoclar Vivadent, Inc.K260682Bond-PR™ Universal AdhesivePremier Dental Products CompanyK251587VITA VMLC PrimerVita Zahnfabrik H. Rauter GmbH & Co. Kg.

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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