AIA-PACK BMG— 510(k) K900440

Substantially Equivalent

Tosoh Medics, Inc.

FDA 510(k) clearance K900440 for AIA-PACK BMG, Substantially Equivalent on 1990-02-26. Applicant: Tosoh Medics, Inc.. Device class: 2.

Clearance details

Applicant
Tosoh Medics, Inc.
Product code
Code JZG
Device class
Class 2
Regulation
21 CFR 866.5630
Advisory panel
Immunology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Washington, D.C., DC, US
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