510(k) K863100
K863100 is an FDA 510(k) premarket notification submitted by Honeywell, Inc. for the device "CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR". The FDA issued a decision of Substantially Equivalent on February 3, 1987. The device falls under product code DPS (Electrocardiograph), a Class II device regulated under 21 CFR 870.2340. Honeywell, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 3, 1987
- Date Received
- August 13, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrocardiograph
- Device Class
- Class II
- Regulation Number
- 870.2340
- Review Panel
- CV
- Submission Type