Last synced on 20 May 2022 at 11:05 pm

FI-10P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951195
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1995
Days to Decision
21 days
Submission Type
Summary

FI-10P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951195
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1995
Days to Decision
21 days
Submission Type
Summary