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FE-24X, FIBER ESOPHAGOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951197
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/1995
Days to Decision
75 days
Submission Type
Summary

FE-24X, FIBER ESOPHAGOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951197
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/1995
Days to Decision
75 days
Submission Type
Summary