FDA Device Establishments · JSON-LD · Markdown

ABBOTT MEDICAL

FEI 3013288201 · Complaint File Establishment per 21 CFR 820.198 · Status: Active

FEI Number3013288201
Owner / OperatorABBOTT LABORATORIES (#1415939)
Address14901 Deveau Pl. Building 2, Minnetonka, MN, US
Registration expiry2026
Initial importer flagN
Registered products5
Product codes (top 20)NVZ, DTB, DXY, NVY, NVN
Regulation § (21 CFR)870.3680, 870.3610
Proprietary namesSuture Sleeve Accessory DS2A088; UltiPace Bradycardia Pacing Lead Model LPA1231; Tendril SDX, Tendril ST, Tendril STS, OptiSense, Tendril DX Leads

External sources

Source: openFDA. Public-domain (CC0).