DeviceClearance

NIDEK STEREO DISC CAMERA(3-DX)/NIDEK STEREO FUNDUS CAMERA(3-DXF)— 510(k) K973533

Substantially Equivalent

Nidek, Inc.

FDA 510(k) clearance K973533 for NIDEK STEREO DISC CAMERA(3-DX)/NIDEK STEREO FUNDUS CAMERA(3-DXF), Substantially Equivalent on 1997-11-04. Applicant: Nidek, Inc..

Clearance details

Applicant
Nidek, Inc.
Product code
Code HKI
Advisory panel
Ophthalmic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Fremont, CA, US
Download summary PDFView on FDA.gov ↗

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