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LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903160
510(k) Type
Traditional
Applicant
CONTINENTAL X-RAY CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/1990
Days to Decision
21 days

LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903160
510(k) Type
Traditional
Applicant
CONTINENTAL X-RAY CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/1990
Days to Decision
21 days