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FDA 510(k)

ZACT DENTAL ARCH TOOTHBRUSCH

K-Number: K833815 · 1984-02-10

Decision Date1984-02-10
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZACT DENTAL ARCH TOOTHBRUSCH is the device name listed in this FDA 510(k) record. The listed applicant is Jfc International, Inc.. It received FDA 510(k) clearance on 1984-02-10 under 510(k) number K833815. The device is classified under product code EFW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZACT DENTAL ARCH TOOTHBRUSCH?

ZACT DENTAL ARCH TOOTHBRUSCH is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Jfc International, Inc.. The 510(k) number is K833815.

When did ZACT DENTAL ARCH TOOTHBRUSCH receive FDA 510(k) clearance?

ZACT DENTAL ARCH TOOTHBRUSCH received FDA 510(k) clearance on 1984-02-10, under 510(k) number K833815.

Who is the listed applicant for ZACT DENTAL ARCH TOOTHBRUSCH?

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

What is the FDA product code for ZACT DENTAL ARCH TOOTHBRUSCH?

The FDA product code for ZACT DENTAL ARCH TOOTHBRUSCH is EFW.

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.

Related Devices (Code: EFW)

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.

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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