Last synced on 20 December 2024 at 11:05 pm

ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981398
510(k) Type
Traditional
Applicant
INTERNEURON PHARMACEUTICALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1998
Days to Decision
45 days
Submission Type
Summary

ANATOMARK NONINVASIVE HEAD REFERENCE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981398
510(k) Type
Traditional
Applicant
INTERNEURON PHARMACEUTICALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1998
Days to Decision
45 days
Submission Type
Summary