Medical Device Manufacturer · CA , Canada

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

2 submissions · 2 cleared · Since 1986

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Peleg Intl. Co. Neurology ✕

2 devices

1-2 of 2

Cleared Jun 18, 1986

SKYLARK MODEL 1001 TENS DEVICE

Neurology · 271d

Cleared Jun 18, 1986

SKYLARK GB 1000

Neurology · 79d