510(k) K964315

REMEL STAPH LATEX KIT by Remel, L.P. — Product Code JWX

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