510(k) K971887

BREATH TAKER by Hofa, LLC — Product Code LCN

K971887 is an FDA 510(k) premarket notification submitted by Hofa, LLC for the device "BREATH TAKER". The FDA issued a decision of Substantially Equivalent on June 10, 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
June 10, 1997
Date Received
May 21, 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