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REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS

Page Type
Cleared 510(K)
510(k) Number
K033593
510(k) Type
Traditional
Applicant
CLEAR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2003
Days to Decision
7 days
Submission Type
Summary

REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS

Page Type
Cleared 510(K)
510(k) Number
K033593
510(k) Type
Traditional
Applicant
CLEAR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2003
Days to Decision
7 days
Submission Type
Summary