Positioning Cushion 301002BLK
by Medtec LLC
Positioning Cushion 301002BLK is a Class II device made by Medtec LLC, cleared under FDA 510(k) K060737 on 31 Mar 2006 and listed in FDA GUDID since 2 Aug 2017 (UDI-DI 00841439102220), active (FDA 510(k)), not in commercial distribution (GUDID) as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00841439102220 | Date2 Aug 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK060737 | Date31 Mar 2006 | StatusActive |
Official records
- AccessGUDID record 00841439102220
- FDA 510(k) database K060737
Across registries
- FDA 510(k) K060737 decided 31 Mar 2006 Active
- FDA GUDID UDI-DI 00841439102220 listed 2 Aug 2017 Listed
Timeline
- Cleared FDA 510(k) K060737
- Listed FDA GUDID 00841439102220
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Positioning Cushion
- Generic name
- Radiological headrest
- Model / Ref / Catalog
- 301002BLK
- Primary DI / UDI-DI
- 00841439102220
- 510(k) Number
- FDA product code
- IYE
- GMDN term
- Radiological headrest
- Device class
- Class II
- Regulation number
- 892.5050
- GUDID distribution status
- Not in Commercial Distribution
- MRI safety
- MR Safe
- Size
- Length — 9.13 Inch
From the manufacturer
Manufacturer's product page: Vacuum & Positioning Cushions