FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
LOPEZ-HORN CARRIER
K Number: K831312
·
Decision May 25, 1983
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
3
Applicant Total
34
Review Days
33
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Basic Information
- Device Name
- LOPEZ-HORN CARRIER
- K Number
- K831312
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.5740
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Chiron Vision Corp.
- Date Received
- April 22, 1983
- Decision Date
- May 25, 1983
- Product Code
- KYP
- 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 |
|---|---|---|---|
| KYP | Snake Bite Suction Kit | FDA class 1 | General Hospital |
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Other Clearances by Chiron Vision Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K970727 | MPORT FOLDABLE LENS PLACEMENT SYSTEM | Dec 17, 1997 | Substantially Equivalent |
| K972808 | HANSATOME MICROKERATOME | Oct 24, 1997 | Substantially Equivalent |
| K960414 | SYNERGIST POWER PACK | Apr 24, 1996 | Substantially Equivalent |
| K944993 | IOLAB.SITE CD PHACOEMULSIFICATION MODULE | Oct 12, 1995 | Substantially Equivalent |
| K944995 | IOLAB/SITE PERISTALTIC MODULE | Oct 5, 1995 | Substantially Equivalent |
| K951292 | PASSPORT FOLDABLE LENS PLACEMENT SYSTEM | Jun 2, 1995 | Substantially Equivalent |
| K944994 | IOLAB/SITE DISPOSABLE DIAPHRAGM CASSETTE | Mar 14, 1995 | Substantially Equivalent |
| K941550 | AUTOMATIC CORNEAL SHAPER SURGICAL INSTRUMENT | Nov 22, 1994 | Substantially Equivalent |
| K935233 | IOLAB LACRIMAL DUCT CATHETER | Sep 15, 1994 | Substantially Equivalent |
| K925606 | OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS | Aug 29, 1994 | Substantially Equivalent |