FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
HAAG-STREIT SLIT LAMP 900
K Number: K792083
·
Decision Nov 16, 1979
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
13
Applicant Total
43
Review Days
31
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Basic Information
- Device Name
- HAAG-STREIT SLIT LAMP 900
- K Number
- K792083
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4700
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Lumenis, Inc.
- Date Received
- October 16, 1979
- Decision Date
- November 16, 1979
- Product Code
- HRM
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| HRM | Microscope, Operating & Accessories, Ac-Powered, Ophthalmic | FDA class 1 | General, Plastic Surgery |
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