FDA 510(k)
Substantially Equivalent
🇺🇸 United States
INGUINAL COMPRESSIVE DEVICE (ICD)
K Number: K761092
·
Decision Dec 16, 1976
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
7
Review Days
24
Basic Information
- Device Name
- INGUINAL COMPRESSIVE DEVICE (ICD)
- K Number
- K761092
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- MEDICAL ELECTRONIC DEVICES, INC.
- Date Received
- November 22, 1976
- Decision Date
- December 16, 1976
- Advisory Committee
- Unknown
- Review Advisory Committee
- OR
- Third Party
- N
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