FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RETRAX SAFETY SYRINGE
K Number: K901508
·
Decision Jun 14, 1990
Classifications
1
FEI Numbers
553
Registration Numbers
553
Same Product Code
738
Applicant Total
1
Review Days
76
Basic Information
- Device Name
- RETRAX SAFETY SYRINGE
- K Number
- K901508
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5860
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- RETRAX, INC.
- Date Received
- March 30, 1990
- Decision Date
- June 14, 1990
- 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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