510(k) K922388

WATERS(TM) LC MODULE I FOR CLINICAL USE by Millipore Corp. — Product Code LDM

K922388 is an FDA 510(k) premarket notification submitted by Millipore Corp. for the device "WATERS(TM) LC MODULE I FOR CLINICAL USE". The FDA issued a decision of Substantially Equivalent on September 11, 1992. The device falls under product code LDM (Instrumentation, High Pressure Liquid Chromatography), a Class I device regulated under 21 CFR 862.2260. Millipore Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 11, 1992
Date Received
May 20, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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