FDA Device Intelligence
Home › CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO.,LTD › Perimeter

Perimeter

CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO.,LTD · Model SK-950C · UDI-DI 06973211070596

HPT
10
510(k) clearances
3
Adverse events
1
Recalls
67
Facilities

Description

It is an AC-powered or manual device intended to determine the extent of the peripheral visual field of a patient. The device projects light on various points of a curved surface, and the patient indicates whether he or she sees the light

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.