Medical Device Manufacturer · CA , Canada

Peleg Intl. Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1986

Total

Cleared

Denied

Peleg Intl. Co. has 2 FDA 510(k) cleared medical devices. Based in Canada, CA.

Historical record: 2 cleared submissions from 1986 to 1986. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Peleg Intl. Co. Filter by specialty or product code using the sidebar.

Peleg Intl. Co. 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 - Peleg Intl. Co.

2 devices

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