510(k) K904966
K904966 is an FDA 510(k) premarket notification submitted by Datamed, Inc. for the device "DATAMED MODEL 401A TRANSRECIEVER". The FDA issued a decision of Substantially Equivalent on July 18, 1991. The device falls under product code DXH (Transmitters And Receivers, Electrocardiograph, Telephone), a Class II device regulated under 21 CFR 870.2920. Datamed, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 18, 1991
- Date Received
- November 5, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Transmitters And Receivers, Electrocardiograph, Telephone
- Device Class
- Class II
- Regulation Number
- 870.2920
- Review Panel
- CV
- Submission Type