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INTERSPEC APOGEE, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K910049
510(k) Type
Traditional
Applicant
INTERSPEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1991
Days to Decision
112 days

INTERSPEC APOGEE, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K910049
510(k) Type
Traditional
Applicant
INTERSPEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1991
Days to Decision
112 days