Last synced on 14 November 2025 at 11:06 pm

PELVIC ARRAY COIL

Page Type
Cleared 510(K)
510(k) Number
K033753
510(k) Type
Special
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2003
Days to Decision
16 days
Submission Type
Summary

PELVIC ARRAY COIL

Page Type
Cleared 510(K)
510(k) Number
K033753
510(k) Type
Special
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2003
Days to Decision
16 days
Submission Type
Summary