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KINGS BAY PRELUDE ONE STEP HCG COMBO KIT

Page Type
Cleared 510(K)
510(k) Number
K931698
510(k) Type
Traditional
Applicant
KING'S BAY INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1993
Days to Decision
213 days
Submission Type
Summary

KINGS BAY PRELUDE ONE STEP HCG COMBO KIT

Page Type
Cleared 510(K)
510(k) Number
K931698
510(k) Type
Traditional
Applicant
KING'S BAY INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1993
Days to Decision
213 days
Submission Type
Summary