
Douglas James Donaldson Compliance Services
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BIOVISION ENDOCULAR PROBE is an FDA 510(k)-cleared medical device (K905115) manufactured by Douglas James Donaldson Compliance Services. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 10, 1991. Regulation: 8.

Ansell
SKU MSC846624

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McKesson
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Hollister
SKU VM-1270031