Last synced on 25 April 2025 at 11:05 pm

OMEGA ULTRASCAN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954911
510(k) Type
Traditional
Applicant
GYNE-TECH INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1996
Days to Decision
91 days
Submission Type
Statement

OMEGA ULTRASCAN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954911
510(k) Type
Traditional
Applicant
GYNE-TECH INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1996
Days to Decision
91 days
Submission Type
Statement