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RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973892
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1998
Days to Decision
216 days
Submission Type
Summary