Last synced on 25 April 2025 at 11:05 pm

LANTOR CUBE STERILIZER TEST PACK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882756
510(k) Type
Traditional
Applicant
LANTOR GROUP
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/6/1988
Days to Decision
93 days

LANTOR CUBE STERILIZER TEST PACK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882756
510(k) Type
Traditional
Applicant
LANTOR GROUP
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/6/1988
Days to Decision
93 days