Last synced on 20 December 2024 at 11:05 pm

ACCU-VENT(TM) WITH NEEDLE-PRO(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912043
510(k) Type
Traditional
Applicant
CONCORD/PORTEX
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
7/5/1991
Days to Decision
58 days
Submission Type
Statement

ACCU-VENT(TM) WITH NEEDLE-PRO(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912043
510(k) Type
Traditional
Applicant
CONCORD/PORTEX
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
7/5/1991
Days to Decision
58 days
Submission Type
Statement