Last synced on 14 November 2025 at 11:06 pm

POWRSYRINGE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K072345
510(k) Type
Traditional
Applicant
PINYONS MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2007
Days to Decision
31 days
Submission Type
Summary

POWRSYRINGE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K072345
510(k) Type
Traditional
Applicant
PINYONS MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2007
Days to Decision
31 days
Submission Type
Summary