Last synced on 15 September 2023 at 11:04 pm

NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880376
510(k) Type
Traditional
Applicant
GENESIS INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/1988
Days to Decision
20 days

NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880376
510(k) Type
Traditional
Applicant
GENESIS INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/1988
Days to Decision
20 days