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FDA 510(k)

ELECTRO FLOSS

K-Number: K930178 · 1993-07-28

ApplicantArizona Implant Dentistry
Decision Date1993-07-28
Product CodeJET
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ELECTRO FLOSS is the device name listed in this FDA 510(k) record. The listed applicant is Arizona Implant Dentistry. It received FDA 510(k) clearance on 1993-07-28 under 510(k) number K930178. The device is classified under product code JET. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO FLOSS?

ELECTRO FLOSS is a medical device that received FDA 510(k) clearance on 1993-07-28. The listed applicant is Arizona Implant Dentistry. The 510(k) number is K930178.

When did ELECTRO FLOSS receive FDA 510(k) clearance?

ELECTRO FLOSS received FDA 510(k) clearance on 1993-07-28, under 510(k) number K930178.

Who is the listed applicant for ELECTRO FLOSS?

The FDA 510(k) record lists Arizona Implant Dentistry as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRO FLOSS?

The FDA product code for ELECTRO FLOSS is JET.

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Related Devices (Code: JET)

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.

K963747REACH STIM-U-DENT PLAQUE REMOVERS WITH MICRODENT/REACH FLOSS STIKS WITH MICRODENT/REACH FLOSS PICS WITH MICRODENT ETC.Whitehill Manufacturing, Inc.K942633ORAL-B INTERDENTAL WOODSTICKS WITH FLUORIDEOral-B LaboratoriesK911418GUM MASSAGERBurn-Henderson PartnershipK885189MASSAGING PICK FOR ORAL HYGIENEDentek Corp.K890910PLAKOFXimex, Ltd.K883225FLOSSIERichard G. Deniro

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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