Last synced on 4 February 2023 at 10:33 pm

DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012917
510(k) Type
Traditional
Applicant
DYNAREX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/2001
Days to Decision
90 days
Submission Type
Summary

DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012917
510(k) Type
Traditional
Applicant
DYNAREX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/2001
Days to Decision
90 days
Submission Type
Summary