Last synced on 14 November 2025 at 11:06 pm

MULTITRAK-PLUS

Page Type
Cleared 510(K)
510(k) Number
K930894
510(k) Type
Traditional
Applicant
ZYMED MEDICAL INSTRUMENTATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1993
Days to Decision
252 days
Submission Type
Statement

MULTITRAK-PLUS

Page Type
Cleared 510(K)
510(k) Number
K930894
510(k) Type
Traditional
Applicant
ZYMED MEDICAL INSTRUMENTATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1993
Days to Decision
252 days
Submission Type
Statement