510(k) K781488

MVS-MODEL SEU-6, DEU-6 by Dentsply Intl. — Product Code EHZ

K781488 is an FDA 510(k) premarket notification submitted by Dentsply Intl. for the device "MVS-MODEL SEU-6, DEU-6". The FDA issued a decision of Substantially Equivalent on September 27, 1978. The device falls under product code EHZ (Evacuator, Oral Cavity), a Class I device regulated under 21 CFR 872.6640. Dentsply Intl. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 27, 1978
Date Received
August 28, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Evacuator, Oral Cavity
Device Class
Class I
Regulation Number
872.6640
Review Panel
DE
Submission Type