510(k) K827126
K827126 is an FDA 510(k) premarket notification submitted by Tecnomed, Inc. for the device "TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE". The FDA issued a decision of Substantially Equivalent on Mar 5, 1982. Tecnomed, Inc. has 17 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 5, 1982
- Date Received
- Feb 4, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No