510(k) K091964

CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS by Procter & Gamble Co. — Product Code JES

K091964 is an FDA 510(k) premarket notification submitted by Procter & Gamble Co. for the device "CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS". The FDA issued a decision of Substantially Equivalent on September 24, 2009. The device falls under product code JES (Floss, Dental), a Class I device regulated under 21 CFR 872.6390. Procter & Gamble Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 24, 2009
Date Received
July 1, 2009
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Floss, Dental
Device Class
Class I
Regulation Number
872.6390
Review Panel
DE
Submission Type