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EIDOLON ENDOSCOPE COUPLER

Page Type
Cleared 510(K)
510(k) Number
K942141
510(k) Type
Traditional
Applicant
EIDOLON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1994
Days to Decision
24 days
Submission Type
Statement

EIDOLON ENDOSCOPE COUPLER

Page Type
Cleared 510(K)
510(k) Number
K942141
510(k) Type
Traditional
Applicant
EIDOLON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1994
Days to Decision
24 days
Submission Type
Statement