Medical Device Manufacturer · US , Lebanon , PA

Molloy Corp.

1 submissions · 1 cleared · Since 1996

Total

Cleared

Denied

Molloy Corp. — FDA 510(k) Submissions

Molloy Corp. 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 Stylet, Tracheal Tube . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

MOLLOY INTUBATING STYLETTE

K943104 · BSR Stylet, Tracheal Tube · Anesthesiology

Apr 1996 659d

Molloy Corp.

Molloy Corp. — FDA 510(k) Submissions

Filters