FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
EDENTEC MODEL 4700 SCANNER
K Number: K884388
·
Decision Jan 10, 1989
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
86
Applicant Total
18
Review Days
84
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Basic Information
- Device Name
- EDENTEC MODEL 4700 SCANNER
- K Number
- K884388
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 870.2810
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Edentec Corp.
- Date Received
- October 18, 1988
- Decision Date
- January 10, 1989
- Product Code
- DSF
- 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 |
|---|---|---|---|
| DSF | Recorder, Paper Chart | FDA class 1 | Cardiovascular |
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Other Clearances by Edentec Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K953363 | OXIFLOW DIGITAL RECORDER | Feb 6, 1996 | Substantially Equivalent - Subject to Tracking Reg. |
| K953540 | EEE | Aug 25, 1995 | Substantially Equivalent |
| K921819 | EDENTEC MODEL 3710 I DIGITAL PRINTER | Oct 22, 1993 | Substantially Equivalent |
| K913749 | EDENTRACE AIRFLOW 3171/SLEEP LAB AIRFLOW 3170 | Jul 2, 1992 | Substantially Equivalent |
| K910871 | EDENTEC DIGITAL CHARTER MODEL 3710 | Aug 29, 1991 | Substantially Equivalent |
| K910870 | EDENTEC MODEL 3711 DIGITAL RECORDER | Aug 29, 1991 | Substantially Equivalent |
| K905575 | MODIFIED MODELS 2000W AND 2000W OPTION H APNEA MON | Jun 20, 1991 | Substantially Equivalent |
| K901060 | EDENTEC MODEL 2000W SYSTEM 700 MONITOR | May 15, 1990 | Substantially Equivalent |
| K893561 | EDENTRACE 670 SYSTEM MULTICHANNEL RECORDER W/OXIM. | Aug 25, 1989 | Substantially Equivalent |
| K892227 | EDENTEC MODEL 2001 MODULAR MEMORY UNIT (MMU) | Jun 20, 1989 | Substantially Equivalent |