FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LITE-TOUCH SYRINGE
K Number: K983430
·
Decision Feb 9, 1999
Classifications
1
FEI Numbers
553
Registration Numbers
553
Same Product Code
738
Applicant Total
3
Review Days
133
Basic Information
- Device Name
- LITE-TOUCH SYRINGE
- K Number
- K983430
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5860
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- MEDICORE, INC.
- Date Received
- September 29, 1998
- Decision Date
- February 9, 1999
- Product Code
- FMF
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FMF | Syringe, Piston | FDA class 2 | General Hospital |
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