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'HILT-WAY' RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880241
510(k) Type
Traditional
Applicant
MEDIFIELD LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/31/1988
Days to Decision
71 days

'HILT-WAY' RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880241
510(k) Type
Traditional
Applicant
MEDIFIELD LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/31/1988
Days to Decision
71 days