510(k) K800210

TONGUE HOLDER/SALIVA EJECTOR by Unitek Corp. — Product Code DYN

K800210 is an FDA 510(k) premarket notification submitted by Unitek Corp. for the device "TONGUE HOLDER/SALIVA EJECTOR". The FDA issued a decision of Substantially Equivalent on February 6, 1980. The device falls under product code DYN (Mouthpiece, Saliva Ejector), a Class I device regulated under 21 CFR 872.6640. Unitek Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 6, 1980
Date Received
February 1, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mouthpiece, Saliva Ejector
Device Class
Class I
Regulation Number
872.6640
Review Panel
DE
Submission Type