FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ALCON FLUID INJECTOR
K Number: K882723
·
Decision Nov 8, 1988
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
2
Applicant Total
47
Review Days
130
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Basic Information
- Device Name
- ALCON FLUID INJECTOR
- K Number
- K882723
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1670
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Alcon Laboratories
- Date Received
- July 1, 1988
- Decision Date
- November 8, 1988
- Product Code
- DQF
- Advisory Committee
- Cardiovascular
- 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 |
|---|---|---|---|
| DQF | Actuator, Syringe, Injector Type | FDA class 2 | Cardiovascular |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (DQF), ordered by most recent decision date.
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Other Clearances by Alcon Laboratories
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|---|---|---|---|
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| K000148 | RGP MULTI-PURPOSE SOLUTION ID 100136 | Apr 11, 2000 | Substantially Equivalent |
| K984573 | OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP | Sep 16, 1999 | Substantially Equivalent |
| K990480 | OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVER | May 10, 1999 | Substantially Equivalent |
| K984575 | MULTI-PURPOSE DISINFECTING SOLUTION ID 90746 | Jan 14, 1999 | Substantially Equivalent |
| K983973 | OPTI-ONE MULTI-PURPOSE SOLUTION | Dec 18, 1998 | Substantially Equivalent |
| K983780 | MULTI-PURPOSE DISINFECTING SOLUTION ID 90746 | Dec 18, 1998 | Substantially Equivalent |
| K981561 | LIQUID ENZYME ID 90133 | Jul 24, 1998 | Substantially Equivalent |
| K981571 | MONARCH IOL DELIVERY SYSTEM | Jul 9, 1998 | Substantially Equivalent |