510(k) K913387
K913387 is an FDA 510(k) premarket notification submitted by Synectics-Dantec for the device "DIGITRAPPER MARK III". The FDA issued a decision of Substantially Equivalent on December 27, 1991. The device falls under product code FFT (Electrode, Ph, Stomach), a Class I device regulated under 21 CFR 876.1400. Synectics-Dantec has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 27, 1991
- Date Received
- July 29, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrode, Ph, Stomach
- Device Class
- Class I
- Regulation Number
- 876.1400
- Review Panel
- GU
- Submission Type