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OMNITRON NEEDLE APPLICATORS 18 AND 21 GAUGE

Page Type
Cleared 510(K)
510(k) Number
K920431
510(k) Type
Traditional
Applicant
OMNITRON INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/1992
Days to Decision
116 days
Submission Type
Statement

OMNITRON NEEDLE APPLICATORS 18 AND 21 GAUGE

Page Type
Cleared 510(K)
510(k) Number
K920431
510(k) Type
Traditional
Applicant
OMNITRON INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/1992
Days to Decision
116 days
Submission Type
Statement