510(k) K914896
- Device
- FRIEDMANN ANALYSER 3
- Applicant
- CLEMENT CLARKE, INC.
- 510(k) number
- K914896
- Product code
- HOK
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1992-01-23
- Date received
- 1991-10-31
- Regulation
- 886.1810
- Classification name
- Screen, Tangent, Projection, Ac-powered
- Medical specialty
- Ophthalmic
- Review panel
- Ophthalmic
- Device class
- 1
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- MICHAEL J WILKINSON
- Address
- Airmed House, Edinburgh Way Harlow, Essex Cm20 2ed England GB
FDA Registration Numbers#
- 3037012186
- 3010363281
- 3010755771
- 3017181414
- 3010373263
Source Documents#
Legacy Summary#
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FDA Review#
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