FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ESA BIOSCIENCES INC. VITAMIN D HPLC TEST

K Number: K072536 · Decision May 7, 2008
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
45
Applicant Total
2
Review Days
243

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ESA BIOSCIENCES INC. VITAMIN D HPLC TEST
K Number
K072536
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1825
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Esa Biosciences, Inc.
Date Received
September 7, 2007
Decision Date
May 7, 2008
Product Code
MRG
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MRG System, Test, Vitamin D

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MRG), ordered by most recent decision date.

View all

Other Clearances by Esa Biosciences, Inc.

K Number Device Name
K052549 LEADCARE II BLOOD LEAD TESTING SYSTEM