510(k) K850125
K850125 is an FDA 510(k) premarket notification submitted by Philips Medical Systems (Cleveland), Inc. for the device "MULTI-SIZE CASSETTE HOLDER". The FDA issued a decision of Substantially Equivalent on March 26, 1985. The device falls under product code IXY (Holder, Radiographic Cassette, Wall-Mounted), a Class I device regulated under 21 CFR 892.1880. Philips Medical Systems (Cleveland), Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 26, 1985
- Date Received
- January 14, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Holder, Radiographic Cassette, Wall-Mounted
- Device Class
- Class I
- Regulation Number
- 892.1880
- Review Panel
- RA
- Submission Type