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INTERSURGICAL HEATED WIRE BREATHING SYSTEMS AND HUMIDIFICATION CHAMBERS, MODEL 2026,2026-CH, 2310, 2320, 2330

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092129
510(k) Type
Traditional
Applicant
INTERSURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2010
Days to Decision
307 days
Submission Type
Summary

INTERSURGICAL HEATED WIRE BREATHING SYSTEMS AND HUMIDIFICATION CHAMBERS, MODEL 2026,2026-CH, 2310, 2320, 2330

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092129
510(k) Type
Traditional
Applicant
INTERSURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2010
Days to Decision
307 days
Submission Type
Summary