FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SPECTROPHOTOMETER ANALYSIS SYS., AA-375

K Number: K770444 · Decision Apr 8, 1977
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
28
Applicant Total
86
Review Days
32

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Basic Information

Device Name
SPECTROPHOTOMETER ANALYSIS SYS., AA-375
K Number
K770444
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2850
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Varian Assoc., Inc.
Date Received
March 7, 1977
Decision Date
April 8, 1977
Product Code
JXR
Advisory Committee
Clinical Chemistry
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
JXR Atomic Absorption Spectrophotometer, General Use

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