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PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE

Page Type
Cleared 510(K)
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)
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