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MICROTEK MINI-MAX DRILL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874535
510(k) Type
Traditional
Applicant
MICROTEK MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1987
Days to Decision
20 days

MICROTEK MINI-MAX DRILL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874535
510(k) Type
Traditional
Applicant
MICROTEK MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1987
Days to Decision
20 days