FLOSS PLUS— 510(k) K931353

Substantially Equivalent

Floss Plus, Inc.

FDA 510(k) clearance K931353 for FLOSS PLUS, Substantially Equivalent on 1993-07-27. Applicant: Floss Plus, Inc.. Device class: 1.

Clearance details

Applicant: Floss Plus, Inc.
Product code: Code JES
Device class: Class 1
Regulation: 21 CFR 872.6390
Advisory panel: Dental
Date received: 1993-03-17
Decision date: 1993-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Muskego, WI, US

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K944034 — PERIO-MED DENTAL FLOSS1995-07-25
K952091 — VUTLER G.U.M. WITH FLUORIDE1995-06-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.