510(k) K905789

FRANKLIN 9000 WALL STAND by Mallinckrodt Group, Inc. — Product Code KPX

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