Medical Device Manufacturer · CA , Winnipeg, Manitoba

Accufast, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2001

Total

Cleared

Denied

Accufast, Inc. has 1 FDA 510(k) cleared medical devices. Based in Winnipeg, Manitoba, CA.

Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Accufast, Inc. Filter by specialty or product code using the sidebar.

Accufast, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Accufast, Inc.

1 devices

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