FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PRECISION CAPILLARIES FOR MICROMANIPULATION
K Number: K024302
·
Decision Feb 19, 2003
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
25
Applicant Total
1
Review Days
57
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Basic Information
- Device Name
- PRECISION CAPILLARIES FOR MICROMANIPULATION
- K Number
- K024302
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.6130
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Brinkmann Instruments, Inc.
- Date Received
- December 24, 2002
- Decision Date
- February 19, 2003
- Product Code
- MQH
- Advisory Committee
- Obstetrics/Gynecology
- Review Advisory Committee
- OB
- 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 |
|---|---|---|---|
| MQH | Microtools, Assisted Reproduction (Pipettes) | FDA class 2 | Obstetrics/Gynecology |
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