510(k) K922388
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