IMMULON 1 EIA TUBES, IMMULON 2 EIA TUBES— 510(k) K854423

Substantially Equivalent

Dynatech Laboratories, Inc.

FDA 510(k) clearance K854423 for IMMULON 1 EIA TUBES, IMMULON 2 EIA TUBES, Substantially Equivalent on 1985-11-20. Applicant: Dynatech Laboratories, Inc.. Device class: 1.

Clearance details

Applicant
Dynatech Laboratories, Inc.
Product code
Code LIB
Device class
Class 1
Regulation
21 CFR 866.2660
Advisory panel
Microbiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Alexandria, VA, US
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