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PSG(TM) 20 GUAGE DOPPLER NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K913941
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1992
Days to Decision
176 days
Submission Type
Statement

PSG(TM) 20 GUAGE DOPPLER NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K913941
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1992
Days to Decision
176 days
Submission Type
Statement