510(k) K870701

KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL by Eastman Kodak Company — Product Code JAC

K870701 is an FDA 510(k) premarket notification submitted by Eastman Kodak Company for the device "KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL". The FDA issued a decision of Substantially Equivalent on February 26, 1987. The device falls under product code JAC (System, X-Ray, Film Marking, Radiographic), a Class I device regulated under 21 CFR 892.1640. Eastman Kodak Company has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 26, 1987
Date Received
February 20, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, X-Ray, Film Marking, Radiographic
Device Class
Class I
Regulation Number
892.1640
Review Panel
RA
Submission Type