Last synced on 30 September 2022 at 11:05 pm

CRANIOCAP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000861
510(k) Type
Traditional
Applicant
GILLETTE CHILDREN'S SPECIALTY HEALTHCARE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2000
Days to Decision
227 days
Submission Type
Summary

CRANIOCAP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000861
510(k) Type
Traditional
Applicant
GILLETTE CHILDREN'S SPECIALTY HEALTHCARE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2000
Days to Decision
227 days
Submission Type
Summary