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ANGIOTEC SPX SPLIT SCREEN DUAL CHANNEL SCAN CONV.

Page Type
Cleared 510(K)
510(k) Number
K893476
510(k) Type
Traditional
Applicant
ANDROS ANALYZERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1989
Days to Decision
50 days

ANGIOTEC SPX SPLIT SCREEN DUAL CHANNEL SCAN CONV.

Page Type
Cleared 510(K)
510(k) Number
K893476
510(k) Type
Traditional
Applicant
ANDROS ANALYZERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1989
Days to Decision
50 days