Kahn-Tact U.S.A., Eff Laryngoscope

Q: What is the product code of K872480?

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

FDA 510(k) K872480 · Effner and Spreine Co.

Substantially Equivalent

510(k) numberK872480

Submission

Device name: Kahn-Tact U.S.A., Eff Laryngoscope
Applicant: Effner and Spreine Co.
Oak Brook, IL, US
Received: June 23, 1987
Decision date: August 10, 1987
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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K984101	FlexibladeCCW · Traditional	Arco Medic , Ltd.	09/03/1999SE

More from Arco Medic , Ltd.

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K875260	Effner Cautery InstrumentsHQP · Traditional	06/06/1988SE
K874755	Effner Fe-Ex* OrogastricKNT · Traditional	04/06/1988SE
K852014	Effner Sims Rectal Speculum W/Fiber Optic IlluminaKOA · Traditional	08/07/1985SE

Questions and answers

When was Kahn-Tact U.S.A., Eff Laryngoscope cleared by the FDA?

Kahn-Tact U.S.A., Eff Laryngoscope (K872480) received a 510(k) decision of Substantially Equivalent on August 10, 1987, 48 days after the submission was received.

What is the product code of K872480?

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