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LFRE INDIRECT LARYNGOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K023004
510(k) Type
Traditional
Applicant
ASTRALITE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2003
Days to Decision
141 days
Submission Type
Summary

LFRE INDIRECT LARYNGOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K023004
510(k) Type
Traditional
Applicant
ASTRALITE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2003
Days to Decision
141 days
Submission Type
Summary