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BIOJECTOR 2000 MODEL 1B02000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960373
510(k) Type
Traditional
Applicant
Bioject, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1997
Days to Decision
404 days
Submission Type
Summary

BIOJECTOR 2000 MODEL 1B02000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960373
510(k) Type
Traditional
Applicant
Bioject, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1997
Days to Decision
404 days
Submission Type
Summary