510(k) K870718

AMERICAN ALCOHOL PREP PAD STERILE MEDIUM by Span-America Medical Systems, Inc. — Product Code LKB

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