DR FLOSSER, FLOSSING AID/FLOSS HOLDING DEVICE— 510(k) K871393

Name: FDA 510(k) clearance K871393
Creator: U.S. Food and Drug Administration
Published: 1987-04-15

Substantially Equivalent

Flossrite Corp.

FDA 510(k) clearance K871393 for DR FLOSSER, FLOSSING AID/FLOSS HOLDING DEVICE, Substantially Equivalent on 1987-04-15. Applicant: Flossrite Corp.. Device class: 1.

Clearance details

Applicant: Flossrite Corp.
Product code: Code JES
Device class: Class 1
Regulation: 21 CFR 872.6390
Advisory panel: Dental
Date received: 1987-04-07
Decision date: 1987-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Wayne, IN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JES

view all

K091964 — CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS2009-09-24
K964976 — FLOSSBRUSH WITH FLUORIDE1997-05-06
K963746 — IDS DENTAL FLOSS WITH SODIUM FLUORIDE MICRODENT DENTAL FLOSS WITH SODIUM FLUORIDE AP-24 DENTAL FLOSS WITH SODIUM FLUORID1996-12-12
K944034 — PERIO-MED DENTAL FLOSS1995-07-25
K952091 — VUTLER G.U.M. WITH FLUORIDE1995-06-28

More clearances from Flossrite Corp.

view all

K871392 — DR FLOSSER REFILL1987-04-15

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