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FDA 510(k)

FLOSSIE

K-Number: K883225 · 1988-08-30

ApplicantRichard G. Deniro
Decision Date1988-08-30
Product CodeJET
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLOSSIE is the device name listed in this FDA 510(k) record. The listed applicant is Richard G. Deniro. It received FDA 510(k) clearance on 1988-08-30 under 510(k) number K883225. 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 FLOSSIE?

FLOSSIE is a medical device that received FDA 510(k) clearance on 1988-08-30. The listed applicant is Richard G. Deniro. The 510(k) number is K883225.

When did FLOSSIE receive FDA 510(k) clearance?

FLOSSIE received FDA 510(k) clearance on 1988-08-30, under 510(k) number K883225.

Who is the listed applicant for FLOSSIE?

The FDA 510(k) record lists Richard G. Deniro as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOSSIE?

The FDA product code for FLOSSIE 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 LaboratoriesK930178ELECTRO FLOSSArizona Implant DentistryK911418GUM MASSAGERBurn-Henderson PartnershipK885189MASSAGING PICK FOR ORAL HYGIENEDentek Corp.K890910PLAKOFXimex, Ltd.

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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