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KEC-3840L/F, VIDEO COLONOSCOPE (*L OR F IN MODEL NUMBER DENOTES LENGTH)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961570
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1996
Days to Decision
62 days
Submission Type
Summary

KEC-3840L/F, VIDEO COLONOSCOPE (*L OR F IN MODEL NUMBER DENOTES LENGTH)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961570
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1996
Days to Decision
62 days
Submission Type
Summary