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SHROUDED NEEDLE DEVICES

Page Type
Cleared 510(K)
510(k) Number
K924718
510(k) Type
Traditional
Applicant
IMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1993
Days to Decision
270 days
Submission Type
Statement

SHROUDED NEEDLE DEVICES

Page Type
Cleared 510(K)
510(k) Number
K924718
510(k) Type
Traditional
Applicant
IMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1993
Days to Decision
270 days
Submission Type
Statement