SYNERMED LDH REAGENT KIT— 510(k) K903773

Substantially Equivalent

Synermed, Inc.

FDA 510(k) clearance K903773 for SYNERMED LDH REAGENT KIT, Substantially Equivalent on 1990-10-12. Applicant: Synermed, Inc.. Device class: 2.

Clearance details

Applicant
Synermed, Inc.
Product code
Code CFJ
Device class
Class 2
Regulation
21 CFR 862.1440
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Quebec, CA
Download summary PDFView on FDA.gov ↗

Recent devices under product code CFJ

view all

More clearances from Synermed, Inc.

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.