Medical Device Manufacturer · US , Orchard Park , NY

Vector, Inc.

1 submissions · 1 cleared · Since 1996

Total

Cleared

Denied

Vector, Inc. — FDA 510(k) Submissions

Vector, Inc. has submitted 1 FDA 510(k) premarket notifications since 1996, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mask, Oxygen . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

FIRST AID KIT(S)

K963298 · BYG Mask, Oxygen · Anesthesiology

Nov 1996 77d

Vector, Inc.

Vector, Inc. — FDA 510(k) Submissions

Filters