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PULMOLIFE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061283
510(k) Type
Traditional
Applicant
MICRO MEDICAL, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/14/2006
Days to Decision
220 days
Submission Type
Summary

PULMOLIFE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061283
510(k) Type
Traditional
Applicant
MICRO MEDICAL, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/14/2006
Days to Decision
220 days
Submission Type
Summary