
Fehling Surgical Instruments, Inc.
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SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe is an FDA 510(k)-cleared medical device (K220981) manufactured by Fehling Surgical Instruments, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 19, 2023. Regulation: 8.

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