Last synced on 30 September 2022 at 11:05 pm

LERMAN & SON CRANIAL ORTHOSIS HELMET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012830
510(k) Type
Traditional
Applicant
LERMAN & SON
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2001
Days to Decision
89 days
Submission Type
Summary

LERMAN & SON CRANIAL ORTHOSIS HELMET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012830
510(k) Type
Traditional
Applicant
LERMAN & SON
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2001
Days to Decision
89 days
Submission Type
Summary