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MODIFIED SITE POWER HANDPIECE II

Page Type
Cleared 510(K)
510(k) Number
K932600
510(k) Type
Traditional
Applicant
CHIRON VISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1994
Days to Decision
242 days
Submission Type
Summary

MODIFIED SITE POWER HANDPIECE II

Page Type
Cleared 510(K)
510(k) Number
K932600
510(k) Type
Traditional
Applicant
CHIRON VISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1994
Days to Decision
242 days
Submission Type
Summary