510(k) K801217

SKIL-CARE GEL WEDGE, FLOTATION PAD by Skil-Care Corp. — Product Code KIC

K801217 is an FDA 510(k) premarket notification submitted by Skil-Care Corp. for the device "SKIL-CARE GEL WEDGE, FLOTATION PAD". The FDA issued a decision of Substantially Equivalent on May 30, 1980. The device falls under product code KIC (Cushion, Flotation), a Class I device regulated under 21 CFR 890.3175. Skil-Care Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 30, 1980
Date Received
May 21, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cushion, Flotation
Device Class
Class I
Regulation Number
890.3175
Review Panel
PM
Submission Type