Laryngoscope Blade (Robertshaw Style)

FDA 510(k) K884073 · Eastmed Enterprises, Inc.

Substantially Equivalent

510(k) numberK884073

Submission

Device name
Laryngoscope Blade (Robertshaw Style)
Applicant
Eastmed Enterprises, Inc.
Marlton, NJ, US
Received
September 27, 1988
Decision date
October 13, 1988
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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K062230MR Fiber Optic Intubating Laryngoscope Handle, Short, Model 310002CCW · Special Minrad, Inc.08/31/2006SE
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K984101FlexibladeCCW · Traditional Arco Medic , Ltd.09/03/1999SE

More from Arco Medic , Ltd.

510(k)DeviceDecision
K922019Laryngoscope RigidCCW · Traditional 01/26/1993SE
K921128Endotracheal Tube StyletBSR · Traditional 06/02/1992SE
K914741Amer Profile Miller Laryngoscope Blades, ModifiedCCW · Traditional 02/03/1992SE
K903618Robertazzi Nasopharyngeal AirwayBTQ · Traditional 01/08/1991SE
K901489Macintosh Laryngoscope Blades (American Profile)CCW · Traditional 04/10/1990SE
K890342Airways (Guedel, Berman & Nasopharyngeal Types)BTO · Traditional 04/27/1989SE
K884584Tongue Seizing Forceps with & Without Rubber PadsBWB · Traditional 11/14/1988SE
K88407215 Millimeter Male and Female AdaptersCAI · Traditional 10/07/1988SE
K882433Laryngoscope RigidCCW · Traditional 09/02/1988SE
K882434Mask, Gas, AnestheticBSJ · Traditional 06/30/1988SE

Questions and answers

When was Laryngoscope Blade (Robertshaw Style) cleared by the FDA?

Laryngoscope Blade (Robertshaw Style) (K884073) received a 510(k) decision of Substantially Equivalent on October 13, 1988, 16 days after the submission was received.

What is the product code of K884073?

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