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PORTA-RESP MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K943146
510(k) Type
Traditional
Applicant
S & M INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1994
Days to Decision
151 days
Submission Type
Summary

PORTA-RESP MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K943146
510(k) Type
Traditional
Applicant
S & M INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1994
Days to Decision
151 days
Submission Type
Summary