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CHILLBUSTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022903
510(k) Type
Traditional
Applicant
MICROTEK MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/2002
Days to Decision
85 days
Submission Type
Summary

CHILLBUSTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022903
510(k) Type
Traditional
Applicant
MICROTEK MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/2002
Days to Decision
85 days
Submission Type
Summary