510(k) K941858
K941858 is an FDA 510(k) premarket notification submitted by Hollister, Inc. for the device "GEL CUSHION". The FDA issued a decision of Substantially Equivalent on May 5, 1994. The device falls under product code KIC (Cushion, Flotation), a Class I device regulated under 21 CFR 890.3175. Hollister, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 5, 1994
- Date Received
- April 15, 1994
- 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