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MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882323
510(k) Type
Traditional
Applicant
MEICOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1988
Days to Decision
24 days

MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882323
510(k) Type
Traditional
Applicant
MEICOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1988
Days to Decision
24 days