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STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE)

Page Type
Cleared 510(K)
510(k) Number
K040300
510(k) Type
Traditional
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2004
Days to Decision
23 days
Submission Type
Summary

STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE)

Page Type
Cleared 510(K)
510(k) Number
K040300
510(k) Type
Traditional
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2004
Days to Decision
23 days
Submission Type
Summary