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INSUFFLATION NEEDLE- 120MM, MODEL 900-200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993625
510(k) Type
Traditional
Applicant
GENICON, LC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2000
Days to Decision
238 days
Submission Type
Summary

INSUFFLATION NEEDLE- 120MM, MODEL 900-200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993625
510(k) Type
Traditional
Applicant
GENICON, LC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2000
Days to Decision
238 days
Submission Type
Summary