Last synced on 15 September 2023 at 11:04 pm

SPOT PRO (220V), MODEL 131.099

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022741
510(k) Type
Special
Applicant
NUCLETRON CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2002
Days to Decision
66 days
Submission Type
Summary

SPOT PRO (220V), MODEL 131.099

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022741
510(k) Type
Special
Applicant
NUCLETRON CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2002
Days to Decision
66 days
Submission Type
Summary