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Peleg Intl. Co.

2 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
SKYLARK MODEL 1001 TENS DEVICE (K853898)Peleg Intl. Co.1986-06-18
SKYLARK GB 1000 (K861214)Peleg Intl. Co.1986-06-18

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Every clearance here is in the API, with alerts when new ones post.