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BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883819
510(k) Type
Traditional
Applicant
CIRCON ACMI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1988
Days to Decision
39 days

BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883819
510(k) Type
Traditional
Applicant
CIRCON ACMI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1988
Days to Decision
39 days