BIOPSY ADAPTER H4222W— 510(k) K861050

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K861050 for BIOPSY ADAPTER H4222W, Substantially Equivalent on 1986-04-02. Applicant: General Electric Co.. Device class: 1.

Clearance details

Applicant
General Electric Co.
Product code
Code GDF
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Milwaukee, WI, US
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