FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
COMPUTER ECG TERMINAL
K Number: K771648
·
Decision Sep 20, 1977
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
296
Applicant Total
6
Review Days
22
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Basic Information
- Device Name
- COMPUTER ECG TERMINAL
- K Number
- K771648
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2920
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Compumed, Inc.
- Date Received
- August 29, 1977
- Decision Date
- September 20, 1977
- 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 Compumed, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K984285 | OSTEOGRAM BONE DENSITOMETER | May 19, 1999 | Substantially Equivalent |
| K955708 | COMPUMED DICON CLIENT | Mar 1, 1996 | Substantially Equivalent |
| K863965 | KENZ-ECG 102 | Dec 22, 1986 | Substantially Equivalent |
| K854626 | COMPUMED PULMONARY FUNCTION ANALYZER MODEL 307B | Feb 28, 1986 | Substantially Equivalent |
| K802272 | COMPUTER ECG TERMINAL | Sep 26, 1980 | Substantially Equivalent |