510(k) K780318
K780318 is an FDA 510(k) premarket notification submitted by Transidyne General Corp. for the device "MODULAR SCANNING DENSITOMETER SYS.". The FDA issued a decision of Substantially Equivalent on April 12, 1978. The device falls under product code JQT (Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica), a Class I device regulated under 21 CFR 862.2400. Transidyne General Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 12, 1978
- Date Received
- February 24, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica
- Device Class
- Class I
- Regulation Number
- 862.2400
- Review Panel
- CH
- Submission Type