Last synced on 1 August 2025 at 11:06 pm

RE-NEW LAPAROSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962119
510(k) Type
Traditional
Applicant
MICROLINE PENTAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1996
Days to Decision
70 days
Submission Type
Summary

RE-NEW LAPAROSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962119
510(k) Type
Traditional
Applicant
MICROLINE PENTAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1996
Days to Decision
70 days
Submission Type
Summary