510(k) K941518
K941518 is an FDA 510(k) premarket notification submitted by Dupont Medical Products for the device "DUPONT CRONEX PORTABLE GRID CASSETTE". The FDA issued a decision of Substantially Equivalent on June 6, 1994. The device falls under product code IXA (Cassette, Radiographic Film), a Class II device regulated under 21 CFR 892.1850. Dupont Medical Products has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 6, 1994
- Date Received
- March 30, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cassette, Radiographic Film
- Device Class
- Class II
- Regulation Number
- 892.1850
- Review Panel
- RA
- Submission Type