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PENTAX CYSTOFIBERSCOPE, MODEL FCY-15P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914008
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1992
Days to Decision
123 days
Submission Type
Statement

PENTAX CYSTOFIBERSCOPE, MODEL FCY-15P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914008
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1992
Days to Decision
123 days
Submission Type
Statement