FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
U.S. TECHNOLOGIES, INC. RETRACTABLE SAFETY SYRINGE
K Number: K032247
·
Decision Sep 30, 2003
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
161
Applicant Total
1
Review Days
70
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Basic Information
- Device Name
- U.S. TECHNOLOGIES, INC. RETRACTABLE SAFETY SYRINGE
- K Number
- K032247
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5860
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- U.S. Technologies, Inc.
- Date Received
- July 22, 2003
- Decision Date
- September 30, 2003
- Product Code
- MEG
- 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 |
|---|---|---|---|
| MEG | Syringe, Antistick | FDA class 2 | General Hospital |
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