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SPECTROPHOTOMETER #390

Page Type
Cleared 510(K)
510(k) Number
K832206
510(k) Type
Traditional
Applicant
ABBOTT DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1983
Days to Decision
48 days

SPECTROPHOTOMETER #390

Page Type
Cleared 510(K)
510(k) Number
K832206
510(k) Type
Traditional
Applicant
ABBOTT DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1983
Days to Decision
48 days