FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MEMORYTRACE ATM MODEL 4222
K Number: K941898
·
Decision Jun 26, 1995
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
296
Applicant Total
2
Review Days
434
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Basic Information
- Device Name
- MEMORYTRACE ATM MODEL 4222
- K Number
- K941898
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2920
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Hi-Tronics Designs, Inc.
- Date Received
- April 18, 1994
- Decision Date
- June 26, 1995
- Product Code
- DXH
- 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 |
|---|---|---|---|
| DXH | Transmitters And Receivers, Electrocardiograph, Telephone | FDA class 2 | Cardiovascular |
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Other Clearances by Hi-Tronics Designs, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K973863 | MEMORYTRACE MODEL 4224 AMBULATORY ECG MONITOR | Jan 2, 1998 | Substantially Equivalent |