Last synced on 12 July 2024 at 11:04 pm

AXON MP-1 MICROPOSITIONER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990683
510(k) Type
Traditional
Applicant
AXON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1999
Days to Decision
245 days
Submission Type
Summary

AXON MP-1 MICROPOSITIONER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990683
510(k) Type
Traditional
Applicant
AXON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1999
Days to Decision
245 days
Submission Type
Summary