Product code KES— Pathology

FDA has cleared 3 devices under product code KES between 1977 and 1988, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19881 clearance
• 19871 clearance
• 19771 clearance

• Sakura Finetek U.S.A., Inc.1 clearance
• Harleco1 clearance
• Abco Dealers, Inc.1 clearance

• K882881 — SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPERSakura Finetek U.S.A., Inc.·1988-07-28
• K872874 — MICROSCOPE COVER GLASSESAbco Dealers, Inc.·1987-08-10
• K771925 — KRYSTALONR LIQ. MOUNTING MED.&COVERSLIPHarleco·1977-11-02