Last synced on 11 July 2025 at 11:06 pm

ROTABLATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901206
510(k) Type
Traditional
Applicant
HEART TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1990
Days to Decision
184 days

ROTABLATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901206
510(k) Type
Traditional
Applicant
HEART TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1990
Days to Decision
184 days