FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
AUTOPOLE REGULATOR SYSTEM
K Number: K924999
·
Decision Dec 24, 1992
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
39
Applicant Total
3
Review Days
83
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Basic Information
- Device Name
- AUTOPOLE REGULATOR SYSTEM
- K Number
- K924999
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.4360
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Escalon Trek Medical
- Date Received
- October 2, 1992
- Decision Date
- December 24, 1992
- Product Code
- KYG
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- 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 |
|---|---|---|---|
| KYG | Device, Irrigation, Ocular Surgery | FDA class 1 | Ophthalmic |
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