510(k) K791138

5880 SERIES OF GAS CHROMATOGRAPHS by Hewlett-Packard Co. — Product Code KZQ

K791138 is an FDA 510(k) premarket notification submitted by Hewlett-Packard Co. for the device "5880 SERIES OF GAS CHROMATOGRAPHS". The FDA issued a decision of Substantially Equivalent on July 24, 1979. The device falls under product code KZQ (Chromatography(Gas), Clinical Use), a Class I device regulated under 21 CFR 862.2250. Hewlett-Packard Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 24, 1979
Date Received
June 18, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chromatography(Gas), Clinical Use
Device Class
Class I
Regulation Number
862.2250
Review Panel
TX
Submission Type