Last synced on 14 November 2025 at 11:06 pm

GENESIS

Page Type
Cleared 510(K)
510(k) Number
K942553
510(k) Type
Traditional
Applicant
BURTON MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1994
Days to Decision
23 days
Submission Type
Statement

GENESIS

Page Type
Cleared 510(K)
510(k) Number
K942553
510(k) Type
Traditional
Applicant
BURTON MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1994
Days to Decision
23 days
Submission Type
Statement