FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RETROJECT(TM) ANTI-AIDS SYRINGE W/RETRAC. NEEDLE
K Number: K881980
·
Decision Jun 28, 1988
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
5
Review Days
47
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Basic Information
- Device Name
- RETROJECT(TM) ANTI-AIDS SYRINGE W/RETRAC. NEEDLE
- K Number
- K881980
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5860
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Habley Medical Technology Corp.
- Date Received
- May 12, 1988
- Decision Date
- June 28, 1988
- 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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Other Clearances by Habley Medical Technology Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K955164 | S.A.R.S. II (SEMI-AUTOMATIC-RECONSTITUTING-SYSTEM) | Mar 20, 1996 | Substantially Equivalent |
| K903007 | MIRCAS DENTAL CARTRIDGE SYRINGE AND MIRCAS COVER | Sep 19, 1990 | Substantially Equivalent |
| K880594 | VACUGUARD(TM) | Apr 28, 1988 | Substantially Equivalent |
| K871007 | ANTI NEEDLE STRIKE ANTI DRUG ABUSE HYPO. SYRINGE | Apr 30, 1987 | Substantially Equivalent |