510(k) K812949
K812949 is an FDA 510(k) premarket notification submitted by Radiation Measurements, Inc. for the device "RMI TRANSILLUMINATOR, MODEL 292". The FDA issued a decision of Substantially Equivalent on December 2, 1981. The device falls under product code HJM (Transilluminator, Ac-Powered), a Class II device regulated under 21 CFR 886.1945. Radiation Measurements, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 2, 1981
- Date Received
- October 21, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Transilluminator, Ac-Powered
- Device Class
- Class II
- Regulation Number
- 886.1945
- Review Panel
- OP
- Submission Type