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BRENTWOOD IQMARK DIGITAL SPIROMETER (INCLUDES DISPOSABLE PNEUMOTACH MOUTHPIECES AND 3-LITER CALIBRATION SYRINGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002499
510(k) Type
Traditional
Applicant
BRENTWOOD MEDICAL TECHNOLOGY CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2000
Days to Decision
86 days
Submission Type
Summary

BRENTWOOD IQMARK DIGITAL SPIROMETER (INCLUDES DISPOSABLE PNEUMOTACH MOUTHPIECES AND 3-LITER CALIBRATION SYRINGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002499
510(k) Type
Traditional
Applicant
BRENTWOOD MEDICAL TECHNOLOGY CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2000
Days to Decision
86 days
Submission Type
Summary