Robertazzi Nasopharyngeal Airway

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K903618 ↗

FDA Product Code

BTQ

Device Class

Class I

Regulation

21 CFR Part 868.5100

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Endotracheal Tube Stylet

  Class I

  FDA 510(k) K921128 Active Cleared 2 Jun 1992

• Laryngoscope Blade (Robertshaw Style)

  Class I

  FDA 510(k) K884073 Active Cleared 13 Oct 1988

• Tongue Seizing Forceps with & Without Rubber Pads

  Class I

  FDA 510(k) K884584 Active Cleared 14 Nov 1988

• 15 Millimeter Male and Female Adapters

  Class I

  FDA 510(k) K884072 Active Cleared 7 Oct 1988

• Mask, Gas, Anesthetic

  Class I

  FDA 510(k) K882434 Active Cleared 30 Jun 1988

• Laryngoscope Rigid

  Class I

  FDA 510(k) K882433 Active Cleared 2 Sep 1988

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