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EXTENSION HANDLE FOR ACUTOME PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830037
510(k) Type
Traditional
Applicant
PRECISION MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1983
Days to Decision
89 days

EXTENSION HANDLE FOR ACUTOME PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K830037
510(k) Type
Traditional
Applicant
PRECISION MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1983
Days to Decision
89 days