Last synced on 2 December 2022 at 11:04 pm

GIP/MEDI-GLOBE NEEDLE SYSTEM FOR ULTRASONIC FNA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935844
510(k) Type
Traditional
Applicant
MEDI-GLOBE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1995
Days to Decision
432 days
Submission Type
Summary

GIP/MEDI-GLOBE NEEDLE SYSTEM FOR ULTRASONIC FNA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935844
510(k) Type
Traditional
Applicant
MEDI-GLOBE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1995
Days to Decision
432 days
Submission Type
Summary