Last synced on 30 September 2022 at 11:05 pm

SURGICAL INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833542
510(k) Type
Traditional
Applicant
HIRATA SANGYO CO. USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1983
Days to Decision
62 days

SURGICAL INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833542
510(k) Type
Traditional
Applicant
HIRATA SANGYO CO. USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1983
Days to Decision
62 days