510(k) K895961
K895961 is an FDA 510(k) premarket notification submitted by Cambridge Medical Instruments, Inc. for the device "MODEL MC6500 ELECTROCARDIOGRAPH". The FDA issued a decision of Substantially Equivalent on January 4, 1990. The device falls under product code DSH (Recorder, Magnetic Tape, Medical), a Class II device regulated under 21 CFR 870.2800. Cambridge Medical Instruments, Inc. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 4, 1990
- Date Received
- October 10, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Recorder, Magnetic Tape, Medical
- Device Class
- Class II
- Regulation Number
- 870.2800
- Review Panel
- CV
- Submission Type