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CROSS-CHECKS P

Page Type
Cleared 510(K)
510(k) Number
K972300
510(k) Type
Traditional
Applicant
STERITEC PRODUCTS MFG. CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1998
Days to Decision
279 days
Submission Type
Summary

CROSS-CHECKS P

Page Type
Cleared 510(K)
510(k) Number
K972300
510(k) Type
Traditional
Applicant
STERITEC PRODUCTS MFG. CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1998
Days to Decision
279 days
Submission Type
Summary