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PRE-CHECK C02 DETECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861398
510(k) Type
Traditional
Applicant
ALLEGHANY INTL. MEDICAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1986
Days to Decision
21 days

PRE-CHECK C02 DETECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861398
510(k) Type
Traditional
Applicant
ALLEGHANY INTL. MEDICAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1986
Days to Decision
21 days