510(k) K837513
K837513 is an FDA 510(k) premarket notification submitted by Xerox Corp. for the device "UNKNOWN". The FDA issued a decision of Substantially Equivalent on Jun 13, 1983. Xerox Corp. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 13, 1983
- Date Received
- Apr 25, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No