510(k) K827124
K827124 is an FDA 510(k) premarket notification submitted by Tecnomed, Inc. for the device "RALCO COLLIMATOR, AUTOMATIC, RADIOGRAPHIC". 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