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PEREGRINE WIDE ANGLE LIGHT PIPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940393
510(k) Type
Traditional
Applicant
PEREGRINE SURGICAL LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1994
Days to Decision
219 days
Submission Type
Statement

PEREGRINE WIDE ANGLE LIGHT PIPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940393
510(k) Type
Traditional
Applicant
PEREGRINE SURGICAL LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1994
Days to Decision
219 days
Submission Type
Statement