510(k) K933455

COMPUTED ORAL RADIOLOGY SYSTEM by Schick Technologies, Inc. — Product Code EAP

K933455 is an FDA 510(k) premarket notification submitted by Schick Technologies, Inc. for the device "COMPUTED ORAL RADIOLOGY SYSTEM". The FDA issued a decision of Substantially Equivalent on January 31, 1994. The device falls under product code EAP (Unit, X-Ray, Intraoral), a Class II device regulated under 21 CFR 872.1810. Schick Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 31, 1994
Date Received
July 14, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Unit, X-Ray, Intraoral
Device Class
Class II
Regulation Number
872.1810
Review Panel
RA
Submission Type