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PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940391
510(k) Type
Traditional
Applicant
PEREGRINE SURGICAL LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1994
Days to Decision
133 days
Submission Type
Statement

PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940391
510(k) Type
Traditional
Applicant
PEREGRINE SURGICAL LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1994
Days to Decision
133 days
Submission Type
Statement