510(k) K781379

MODEL 5000, LIQUID CHROMATOGRAPHY by Varian Assoc., Inc. — Product Code KIE

K781379 is an FDA 510(k) premarket notification submitted by Varian Assoc., Inc. for the device "MODEL 5000, LIQUID CHROMATOGRAPHY". The FDA issued a decision of Substantially Equivalent on September 14, 1978. The device falls under product code KIE (Apparatus, High Pressure Liquid Chromatography), a Class I device regulated under 21 CFR 862.2260. Varian Assoc., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 14, 1978
Date Received
August 11, 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