FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LDS MONITORING ELECTRODE
K Number: K821846
·
Decision Jul 30, 1982
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
29
Review Days
38
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Basic Information
- Device Name
- LDS MONITORING ELECTRODE
- K Number
- K821846
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2360
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Life Design Systems, Inc.
- Date Received
- June 22, 1982
- Decision Date
- July 30, 1982
- Product Code
- DRX
- 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 |
|---|---|---|---|
| DRX | Electrode, Electrocardiograph | FDA class 2 | Cardiovascular |
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Other Clearances by Life Design Systems, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K913714 | MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM) | Dec 1, 1992 | Substantially Equivalent |
| K885313 | HUMIDI-FLEX TM | Oct 11, 1989 | Substantially Equivalent |
| K893030 | CHILD SIZE - FILTER FLEX (TM) | Sep 18, 1989 | Substantially Equivalent |
| K892862 | FLEX-CUP PERCUSSOR | May 25, 1989 | Substantially Equivalent |
| K892221 | PULMONARY RESUSCITATOR, MODIFICATION | May 18, 1989 | Substantially Equivalent |
| K890011 | OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING | Mar 20, 1989 | Substantially Equivalent |
| K890108 | MODIFIED CUSHION-FLEX(TM) | Jan 24, 1989 | Substantially Equivalent |
| K884387 | CUSHION FLEX(TM) | Nov 17, 1988 | Substantially Equivalent |
| K884068 | PULMANEX TM (NEO-NATAL SIZE) | Nov 16, 1988 | Substantially Equivalent |
| K873179 | HEATER WIRE BREATHING CIRCUIT | Mar 31, 1988 | Substantially Equivalent |