Last synced on 23 September 2022 at 11:05 pm

KERATOME BLADE, CHIROM MODEL ALK 500500; KERATOME BLADE, S.C.M.D. MODEL TUROKERATOME 400400

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980508
510(k) Type
Traditional
Applicant
MICROSPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1998
Days to Decision
80 days
Submission Type
Summary

KERATOME BLADE, CHIROM MODEL ALK 500500; KERATOME BLADE, S.C.M.D. MODEL TUROKERATOME 400400

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980508
510(k) Type
Traditional
Applicant
MICROSPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1998
Days to Decision
80 days
Submission Type
Summary