Last synced on 30 May 2025 at 11:05 pm

VISITHERM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852950
510(k) Type
Traditional
Applicant
C.D. REGELIN & ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1986
Days to Decision
211 days

VISITHERM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852950
510(k) Type
Traditional
Applicant
C.D. REGELIN & ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1986
Days to Decision
211 days