Last synced on 30 May 2025 at 11:05 pm

ORWO X-RAY FILM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920539
510(k) Type
Traditional
Applicant
BURKHART ROENTGEN INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1992
Days to Decision
146 days
Submission Type
Statement

ORWO X-RAY FILM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920539
510(k) Type
Traditional
Applicant
BURKHART ROENTGEN INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1992
Days to Decision
146 days
Submission Type
Statement