Last synced on 23 September 2022 at 11:05 pm

PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031023
510(k) Type
Traditional
Applicant
PEREGRINE SURGICAL LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2003
Days to Decision
88 days
Submission Type
Summary

PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031023
510(k) Type
Traditional
Applicant
PEREGRINE SURGICAL LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2003
Days to Decision
88 days
Submission Type
Summary