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NEOLINE(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914778
510(k) Type
Traditional
Applicant
MARTECH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
9/16/1992
Days to Decision
329 days
Submission Type
Statement

NEOLINE(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914778
510(k) Type
Traditional
Applicant
MARTECH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
9/16/1992
Days to Decision
329 days
Submission Type
Statement