510(k) K990648
K990648 is an FDA 510(k) premarket notification submitted by Keller Medical Specialties Products, Inc. for the device "KELLER VITAL SIGNS MONITOR, KMS 890+". The FDA issued a decision of Substantially Equivalent on August 10, 1999. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Keller Medical Specialties Products, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 10, 1999
- Date Received
- March 1, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Measurement, Blood-Pressure, Non-Invasive
- Device Class
- Class II
- Regulation Number
- 870.1130
- Review Panel
- CV
- Submission Type