510(k) K870718
K870718 is an FDA 510(k) premarket notification submitted by Span-America Medical Systems, Inc. for the device "AMERICAN ALCOHOL PREP PAD STERILE MEDIUM". The FDA issued a decision of Substantially Equivalent on May 7, 1987. The device falls under product code LKB (Pad, Alcohol, Device Disinfectant), a Class U device. Span-America Medical Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 7, 1987
- Date Received
- February 20, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pad, Alcohol, Device Disinfectant
- Device Class
- Class U
- Regulation Number
- Review Panel
- HO
- Submission Type