510(k) K842056

ELVI 165 PROTEO SEROSKOP by Logos Scientific, Inc. — Product Code JQT

K842056 is an FDA 510(k) premarket notification submitted by Logos Scientific, Inc. for the device "ELVI 165 PROTEO SEROSKOP". The FDA issued a decision of Substantially Equivalent on June 22, 1984. The device falls under product code JQT (Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica), a Class I device regulated under 21 CFR 862.2400. Logos Scientific, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 22, 1984
Date Received
May 22, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica
Device Class
Class I
Regulation Number
862.2400
Review Panel
CH
Submission Type