Last synced on 30 September 2022 at 11:05 pm

VYKER SILICONE EPISTAXIS CATHETER V-27030, VYKER SILICONE EPISTAXIS CATHETER KIT V-2703K

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972922
510(k) Type
Traditional
Applicant
INTERVIEW MEDICAL TECHNOLOGY CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1997
Days to Decision
61 days
Submission Type
Statement

VYKER SILICONE EPISTAXIS CATHETER V-27030, VYKER SILICONE EPISTAXIS CATHETER KIT V-2703K

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972922
510(k) Type
Traditional
Applicant
INTERVIEW MEDICAL TECHNOLOGY CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1997
Days to Decision
61 days
Submission Type
Statement