← Back to catalogue

Model Bbd Breast Immobilization And Biopsy Device

FDA 510(k)

Class II (US FDA 510(k))

510(k) K052704

by Invivo Corp.

Identifiers

510(k) Number
K052704 FDA 510(k)
FDA Product Code
MOS FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 892.1000 FDA 510(k)
Regulation Number
892.1000 FDA 510(k)
Advisory Committee
Radiology FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Model Bbd Breast Immobilization And Biopsy Device by Invivo Corp. — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Invivo Corp.

Sources (1)

  • FDA 510(k) K052704 24 fields · synced Jun 19, 2026