Atlas FDA

PHOTRON VISUAL FIELD ANALYZER

FDA 510(k) clearance K860642 · decided 1986-04-15

Clearance details

K-number
K860642
Device name
PHOTRON VISUAL FIELD ANALYZER
Applicant
Biosan Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1986-02-20
Decision date
1986-04-15
Days to decision
54 days
Clearance type
Traditional
Product code
HOM
Device class
1
Regulation number
886.1810
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
San Rafael, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.