Last synced on 25 April 2025 at 11:05 pm

PEREGRINE STRAIGHT LASER PROBE, MODEL PD6000.00

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024061
510(k) Type
Traditional
Applicant
PEREGRINE SURGICAL LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2003
Days to Decision
88 days
Submission Type
Summary

PEREGRINE STRAIGHT LASER PROBE, MODEL PD6000.00

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024061
510(k) Type
Traditional
Applicant
PEREGRINE SURGICAL LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2003
Days to Decision
88 days
Submission Type
Summary