510(k) K811098
K811098 is an FDA 510(k) premarket notification submitted by Scott Laboratories, Inc. for the device "SERO-STAT STAPHYLOCOCCUS TEST". The FDA issued a decision of Substantially Equivalent on May 5, 1981. The device falls under product code JWX (Kit, Screening, Staphylococcus Aureus), a Class I device regulated under 21 CFR 866.2660. Scott Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 5, 1981
- Date Received
- April 22, 1981
- 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