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NEOLON NEOPRENE SURGICAL GLOVES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954325
510(k) Type
Traditional
Applicant
Maxxim Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/1996
Days to Decision
242 days
Submission Type
Statement

NEOLON NEOPRENE SURGICAL GLOVES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954325
510(k) Type
Traditional
Applicant
Maxxim Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/1996
Days to Decision
242 days
Submission Type
Statement