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GENERAL PURPOSE KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881083
510(k) Type
Traditional
Applicant
MED-DEX INTL.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
4/7/1988
Days to Decision
24 days

GENERAL PURPOSE KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881083
510(k) Type
Traditional
Applicant
MED-DEX INTL.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
4/7/1988
Days to Decision
24 days