510(k) K905789
K905789 is an FDA 510(k) premarket notification submitted by Mallinckrodt Group, Inc. for the device "FRANKLIN 9000 WALL STAND". The FDA issued a decision of Substantially Equivalent on May 20, 1991. The device falls under product code KPX (Changer, Radiographic Film/Cassette), a Class II device regulated under 21 CFR 892.1860. Mallinckrodt Group, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 20, 1991
- Date Received
- December 27, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Changer, Radiographic Film/Cassette
- Device Class
- Class II
- Regulation Number
- 892.1860
- Review Panel
- RA
- Submission Type