510(k) K964315
K964315 is an FDA 510(k) premarket notification submitted by Remel, L.P. for the device "REMEL STAPH LATEX KIT". The FDA issued a decision of Substantially Equivalent on February 7, 1997. The device falls under product code JWX (Kit, Screening, Staphylococcus Aureus), a Class I device regulated under 21 CFR 866.2660. Remel, L.P. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 7, 1997
- Date Received
- October 29, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Screening, Staphylococcus Aureus
- Device Class
- Class I
- Regulation Number
- 866.2660
- Review Panel
- MI
- Submission Type