Atlas FDA

TRUEFIELD ANALYZER

FDA 510(k) clearance K063310 · decided 2007-08-02

Clearance details

K-number
K063310
Device name
TRUEFIELD ANALYZER
Applicant
Seeing Machines Limited
Decision
Substantially Equivalent
Date received
2006-11-02
Decision date
2007-08-02
Days to decision
273 days
Clearance type
Traditional
Product code
HPT
Device class
1
Regulation number
886.1605
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
San Diego, CA, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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KASHA VISUAL FIELD SYSTEM (K971156)Kasha Software, Inc.1997-05-28
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OPTICOM M600 (K932258)Clement Clarke, Inc.1994-07-25
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Recalls involving this device

No recalls on record reference this clearance.