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CLM LARYNGOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K953179
510(k) Type
Traditional
Applicant
PENLON LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/6/1995
Days to Decision
88 days
Submission Type
Summary

CLM LARYNGOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K953179
510(k) Type
Traditional
Applicant
PENLON LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/6/1995
Days to Decision
88 days
Submission Type
Summary