FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DUOPRO SAFETY SYRINGE (DUOPROSS)
K Number: K020623
·
Decision May 2, 2002
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
161
Applicant Total
5
Review Days
65
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Basic Information
- Device Name
- DUOPRO SAFETY SYRINGE (DUOPROSS)
- K Number
- K020623
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5860
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- M.K. Meditech Co. , Ltd.
- Date Received
- February 26, 2002
- Decision Date
- May 2, 2002
- 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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Other Clearances by M.K. Meditech Co. , Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K050131 | INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE | Apr 5, 2005 | Substantially Equivalent |
| K034031 | 10 ML BAK'SNAP DUOPROSS RETRACTABLE SAFETY SYRINGE | Jan 21, 2004 | Substantially Equivalent |
| K031594 | BAK'SNAP DUOPRO SAFETY SYRING (DUOPROSS) SAFETY'TRAY ALLERGY SAFETY SYRINGE TRAY | Jun 6, 2003 | Substantially Equivalent |
| K022806 | DUOPRO SAFETY SYRINGE (DUOPROSS) | Sep 19, 2002 | Substantially Equivalent |