FDA Device Intelligence
Home › KOWA COMPANY,LTD. › KOWA AP-7000

KOWA AP-7000

KOWA COMPANY,LTD. · Model FT10K · UDI-DI 04987646805113

HPT Prescription
10
510(k) clearances
3
Adverse events
1
Recalls
68
Facilities

Description

KOWA AP-7000 is an automatic perimeter to perform perimetry examinations and to display and output examination results. Static quantitative perimetry examinations and kinetic perimetry examinations are available.

Recalls

DateFirmReason
2012-08-17Haag-Streit USA IncThe firm recalled the device after learning of a possible deviation in the stimulus luminance of the Perimeter OCTOPUS 101.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.