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OLYMPUS-KEYMED ENDOSCOPIC CO2 REGULATOR, MODEL ECR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881004
510(k) Type
Traditional
Applicant
KEYMED, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/12/1988
Days to Decision
64 days

OLYMPUS-KEYMED ENDOSCOPIC CO2 REGULATOR, MODEL ECR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881004
510(k) Type
Traditional
Applicant
KEYMED, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/12/1988
Days to Decision
64 days