510(k) K781771

DETECTOR, MODEL 79875A, VARIABLE by Hewlett-Packard Co. — Product Code KIE

K781771 is an FDA 510(k) premarket notification submitted by Hewlett-Packard Co. for the device "DETECTOR, MODEL 79875A, VARIABLE". The FDA issued a decision of Substantially Equivalent on December 20, 1978. The device falls under product code KIE (Apparatus, High Pressure Liquid Chromatography), a Class I device regulated under 21 CFR 862.2260. Hewlett-Packard Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 20, 1978
Date Received
October 13, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, High Pressure Liquid Chromatography
Device Class
Class I
Regulation Number
862.2260
Review Panel
TX
Submission Type