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FDA 510(k)

CEDETA

K-Number: K915717 · 1992-11-23

ApplicantD-W Intl.
Decision Date1992-11-23
Product CodeLWM
DecisionSubstantially Equivalent

Device Summary

CEDETA is the device name listed in this FDA 510(k) record. The listed applicant is D-W Intl.. It received FDA 510(k) clearance on 1992-11-23 under 510(k) number K915717. The device is classified under product code LWM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEDETA?

CEDETA is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is D-W Intl.. The 510(k) number is K915717.

When did CEDETA receive FDA 510(k) clearance?

CEDETA received FDA 510(k) clearance on 1992-11-23, under 510(k) number K915717.

Who is the listed applicant for CEDETA?

The FDA 510(k) record lists D-W Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEDETA?

The FDA product code for CEDETA is LWM.

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Related Devices (Code: LWM)

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.

K193570Dental Pain EraserSynapse DentalK192429Dental Pain EraserSynapse DentalK182947Dental Pain EraserSynapse Dental, LLCK011001TEAM-UP TM DENTAL ELECTRONIC ANESTHESIA SYSTEMSatelecK9353043M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 86703M CompanyK9350853M DENTAL ELECTRONONIC ANESTHESIA (DEA0 SYSTEM 8670 ADDITIONAL APPLICATIONS3M Company

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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