510(k) K000257
K000257 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE 2000 PAP, MODELS L2KPA2, L2KPA6". The FDA issued a decision of Substantially Equivalent on February 23, 2000. The device falls under product code JFH (Acid Phosphatase (Prostatic), Tartrate Inhibited), a Class II device regulated under 21 CFR 862.1020. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 23, 2000
- Date Received
- January 27, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Acid Phosphatase (Prostatic), Tartrate Inhibited
- Device Class
- Class II
- Regulation Number
- 862.1020
- Review Panel
- CH
- Submission Type