FDA 510(k)
Substantially Equivalent
🇺🇸 United States
TLC SUPPORT PRODUCTS
K Number: K803029
·
Decision Dec 22, 1980
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
95
Review Days
26
Basic Information
- Device Name
- TLC SUPPORT PRODUCTS
- K Number
- K803029
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- ORTHOPEDIC SYSTEMS, INC.
- Date Received
- November 26, 1980
- Decision Date
- December 22, 1980
- Advisory Committee
- Unknown
- Review Advisory Committee
- OR
- Third Party
- N
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