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GYNEX EXTENDED REACH NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980238
510(k) Type
Traditional
Applicant
GYNEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1998
Days to Decision
210 days
Submission Type
Summary

GYNEX EXTENDED REACH NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980238
510(k) Type
Traditional
Applicant
GYNEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1998
Days to Decision
210 days
Submission Type
Summary