FDA 510(k)
FDA class 2
Substantially Equivalent
🇦🇺 Australia
BLY-501 ADAPTOR
K Number: K012540
·
Decision Sep 26, 2001
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
6
Review Days
50
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Basic Information
- Device Name
- BLY-501 ADAPTOR
- K Number
- K012540
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.2340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Micromedical Industries, Ltd.
- Date Received
- August 7, 2001
- Decision Date
- September 26, 2001
- Product Code
- DPS
- 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 |
|---|---|---|---|
| DPS | Electrocardiograph | FDA class 2 | Cardiovascular |
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Other Clearances by Micromedical Industries, Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K013311 | MODIFICATION TO: POCKETVIEW ECG SOFTWARE | Jan 3, 2002 | Substantially Equivalent |
| K990266 | MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE | Feb 2, 1999 | Substantially Equivalent |
| K922528 | CMS SYSTEM | May 12, 1995 | Substantially Equivalent |
| K915627 | PACEVIEW | Mar 27, 1992 | Substantially Equivalent |
| K915624 | MODIFIED BIOLOG | Mar 27, 1992 | Substantially Equivalent |