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MARTECH ENDOSCOPIC INJECTION NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K960519
510(k) Type
Traditional
Applicant
MARTECH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1996
Days to Decision
86 days
Submission Type
Summary

MARTECH ENDOSCOPIC INJECTION NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K960519
510(k) Type
Traditional
Applicant
MARTECH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1996
Days to Decision
86 days
Submission Type
Summary