510(k) K842380
K842380 is an FDA 510(k) premarket notification submitted by American Pharmaseal Div. Ahsc for the device "PRESSURE RELIEF SEAT CUSHION". The FDA issued a decision of Substantially Equivalent on June 28, 1984. The device falls under product code KIC (Cushion, Flotation), a Class I device regulated under 21 CFR 890.3175. American Pharmaseal Div. Ahsc has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 28, 1984
- Date Received
- June 18, 1984
- 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