FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PROPAQ 102,104,106,102EL,104EL,&106EL
K Number: K914838
·
Decision Jan 10, 1992
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
424
Applicant Total
15
Review Days
77
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- PROPAQ 102,104,106,102EL,104EL,&106EL
- K Number
- K914838
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1025
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Protocol Systems, Inc.
- Date Received
- October 25, 1991
- Decision Date
- January 10, 1992
- Product Code
- MHX
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MHX | Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA class 2 | Cardiovascular |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (MHX), ordered by most recent decision date.
Radius VSM and Accessories
FDA 510(k)
FDA Class 2
·Cardiovascular
M12 Telemetry System
FDA 510(k)
FDA Class 2
·Cardiovascular
ePM Series Patient Monitor (ePM 10/ePM 10A/ePM 10C/Guardian plus/ ePM 12/ePM 12A/ePM 12C / ePM 15/ePM 15A/ePM 15C /ePM 10M/ ePM 10MA/ ePM 10MC/ePM 12M/ ePM 12MA/ ePM 12MC/ePM 15M/ ePM 15MA/ ePM 15MC)
FDA 510(k)
FDA Class 2
·Cardiovascular
Vista CMS
FDA 510(k)
FDA Class 2
·Cardiovascular
uMEC 60/ uMEC 70/ uMEC 80/uMEC 100/uMEC 120/uMEC 150 Patient Monitors
FDA 510(k)
FDA Class 2
·Cardiovascular
Vista 300/Vista 300 S; Vista 300 Non-Inv Model A, US (2601064); Vista 300 Invasive Model C, US (2601065); Vista 300 S Non-Inv Model A, US (2602425); Vista 300 S Invasive Model B, US (2602426); Vista 300 S Invasive Model C, US (2602427)
FDA 510(k)
FDA Class 2
·Cardiovascular
Other Clearances by Protocol Systems, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K002725 | MICROPAQ, MODELS 402 AND 404 | Nov 21, 2000 | Substantially Equivalent |
| K972121 | ACUITY CENTRAL STATION | Nov 7, 1997 | Substantially Equivalent |
| K951246 | PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONS | Feb 2, 1996 | Substantially Equivalent - Subject to Tracking Reg. |
| K945071 | PROPAQ 200 MONITOR | May 10, 1995 | Substantially Equivalent |
| K935846 | MODEL ACUITY CENTRAL STATION | Dec 5, 1994 | Substantially Equivalent |
| K934711 | PROPAQ ECG TELEMETRY OPTION | Sep 1, 1994 | Substantially Equivalent |
| K921497 | PROPAQ MONITORS, MODIFICATION | Mar 23, 1993 | Substantially Equivalent |
| K913193 | MODEL 100 CENTRAL STATION | Oct 16, 1991 | Substantially Equivalent |
| K910882 | PROPAQ 102EL, 104EL AND 106EL | May 8, 1991 | Substantially Equivalent |
| K910772 | PROPAQ 102, 104 AND 106 | Apr 12, 1991 | Substantially Equivalent |