FRIEDMANN ANALYSER 3
FDA 510(k) clearance K914896 · decided 1992-01-23
Clearance details
- K-number
- K914896
- Device name
- FRIEDMANN ANALYSER 3
- Applicant
- Clement Clarke, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-10-31
- Decision date
- 1992-01-23
- Days to decision
- 84 days
- Clearance type
- Traditional
- Product code
- HOK
- Device class
- 1
- Regulation number
- 886.1810
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- England, GB
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.