Last synced on 23 May 2025 at 11:06 pm

ACCUFUSER; ACCUFUSER PLUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003915
510(k) Type
Traditional
Applicant
HELPTECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2001
Days to Decision
58 days
Submission Type
Summary

ACCUFUSER; ACCUFUSER PLUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003915
510(k) Type
Traditional
Applicant
HELPTECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2001
Days to Decision
58 days
Submission Type
Summary