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MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933659
510(k) Type
Traditional
Applicant
MEDIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1993
Days to Decision
118 days
Submission Type
Statement