510(k) K973175

TONGUE KLEAN by Softek Ent. — Product Code LCN

K973175 is an FDA 510(k) premarket notification submitted by Softek Ent. for the device "TONGUE KLEAN". The FDA issued a decision of Substantially Equivalent on October 14, 1997. The device falls under product code LCN (Scraper, Tongue), a Class I device regulated under 21 CFR 872.6855.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 14, 1997
Date Received
August 25, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Scraper, Tongue
Device Class
Class I
Regulation Number
872.6855
Review Panel
DE
Submission Type