510(k) K895477
K895477 is an FDA 510(k) premarket notification submitted by Nova Health Systems, Inc. for the device "NOVA PILLOW". The FDA issued a decision of Substantially Equivalent on January 10, 1990. The device falls under product code IQK (Orthosis, Cervical), a Class I device regulated under 21 CFR 890.3490. Nova Health Systems, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 10, 1990
- Date Received
- September 11, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Orthosis, Cervical
- Device Class
- Class I
- Regulation Number
- 890.3490
- Review Panel
- PM
- Submission Type