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KERASCAN MODEL 2000 KERATOGRAPHIC AUTO ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864037
510(k) Type
Traditional
Applicant
KERA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1986
Days to Decision
28 days

KERASCAN MODEL 2000 KERATOGRAPHIC AUTO ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864037
510(k) Type
Traditional
Applicant
KERA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1986
Days to Decision
28 days