Last synced on 20 May 2022 at 11:05 pm

TRACHEAL TUBE LASER SHIELD KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883096
510(k) Type
Traditional
Applicant
AMERICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1988
Days to Decision
48 days

TRACHEAL TUBE LASER SHIELD KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883096
510(k) Type
Traditional
Applicant
AMERICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1988
Days to Decision
48 days