Last synced on 16 February 2024 at 11:04 pm

MM-1 MOVEMENT MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971318
510(k) Type
Traditional
Applicant
AXON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1997
Days to Decision
110 days
Submission Type
Statement

MM-1 MOVEMENT MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971318
510(k) Type
Traditional
Applicant
AXON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1997
Days to Decision
110 days
Submission Type
Statement