NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001U— 510(k) K093916

Substantially Equivalent

Perkinelmer, Inc.

FDA 510(k) clearance K093916 for NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001U, Substantially Equivalent on 2010-08-23. Applicant: Perkinelmer, Inc.. Device class: 2.

Clearance details

Applicant
Perkinelmer, Inc.
Product code
Code NQL
Device class
Class 2
Regulation
21 CFR 862.1055
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Indianapolis, IN, US
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