FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AUTOCLIX
K Number: K810075
·
Decision Feb 4, 1981
Classifications
1
FEI Numbers
157
Registration Numbers
157
Same Product Code
109
Applicant Total
21
Review Days
22
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Basic Information
- Device Name
- AUTOCLIX
- K Number
- K810075
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4850
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Biodynamics Corp.
- Date Received
- January 13, 1981
- Decision Date
- February 4, 1981
- Product Code
- FMK
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| FMK | Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Biodynamics Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K051675 | BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER | Mar 16, 2006 | Substantially Equivalent |
| K884033 | BIODYNAMICS MODEL 200 BODY COMPOSITION ANALYZER | Nov 17, 1988 | Substantially Equivalent |
| K881631 | BIODYNAMICS AUTOTRANSFUSION RESERVOIR | Sep 9, 1988 | Substantially Equivalent |
| K881968 | BIODYNAMICS MODEL BI-400 BODY COMPOSITION ANALYZER | Jul 28, 1988 | Substantially Equivalent |
| K874361 | BIODYNAMICS MODEL BI-300 BODY COMPOSITION ANALYZER | Mar 16, 1988 | Substantially Equivalent |
| K873807 | AUTOTRANSFUSION APPARATUS | Mar 9, 1988 | Substantially Equivalent |
| K874034 | ADR-22 AUTOMATIC DIALYZER REPROCESSOR | Oct 23, 1987 | Substantially Equivalent |
| K870052 | INFUMIX MIXING CONTAINER | Feb 27, 1987 | Substantially Equivalent |
| K822716 | UNIVERSAL CENTRIFUGE | Sep 30, 1982 | Substantially Equivalent |
| K822715 | PLATELET CENTRIFUGE | Sep 30, 1982 | Substantially Equivalent |