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ACCU-BEAM TISSUE DRILL & ASPIRATION/INJECTION NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934398
510(k) Type
Traditional
Applicant
TRANSAMERICAN TECHNOLOGIES INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1994
Days to Decision
159 days
Submission Type
Statement