Belscope Laryngoscope

FDA 510(k) K904918 · Avulunga Pty. , Ltd.

Substantially Equivalent

510(k) numberK904918

Submission

Device name
Belscope Laryngoscope
Applicant
Avulunga Pty. , Ltd.
N.S.W., Australia, AU
Received
October 31, 1990
Decision date
July 22, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CCW – Laryngoscope, Rigid
Device class
Class I (low risk)
Regulation
21 CFR 868.5540
Specialty
Anesthesiology

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K062231MR Fiber Optic Intubating Laryngoscope Handle, Standard, Model 310001CCW · Special Minrad, Inc.08/31/2006SE
K062230MR Fiber Optic Intubating Laryngoscope Handle, Short, Model 310002CCW · Special Minrad, Inc.08/31/2006SE
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Questions and answers

When was Belscope Laryngoscope cleared by the FDA?

Belscope Laryngoscope (K904918) received a 510(k) decision of Substantially Equivalent on July 22, 1991, 264 days after the submission was received.

What is the product code of K904918?

The FDA product code is CCW – Laryngoscope, Rigid, a Class I (low risk) device regulated under 21 CFR 868.5540.