Laser Gas Mixtures

FDA 510(k) K820535 · Union Carbide Corp.

Substantially Equivalent

510(k) numberK820535

Submission

Device name
Laser Gas Mixtures
Applicant
Union Carbide Corp.
Mchenry, IL, US
Received
March 2, 1982
Decision date
March 31, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EWG – Laser, Ent Microsurgical Carbon-Dioxide
Device class
Class II (moderate risk)
Regulation
21 CFR 874.4500
Specialty
Ear, Nose, Throat

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K872710Model 20-B W/OB-10A/U Attach. for Ear, Nose/ThroatEWG · Traditional Directed Energy, Inc.09/24/1987SE
K870840Model 20-C W/BR-20A/U Attach/Model HL-3.O AttachEWG · Traditional Directed Energy, Inc.06/12/1987SE
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K862866Model 10-C W/LP-10A/U & OS-10A/U for Oral/Ent UseEWG · Traditional Directed Energy, Inc.01/09/1987SE
K862865Model 10-C W/LP-10A/U & OB-10A/U for Oral/Ent UseEWG · Traditional Directed Energy, Inc.01/09/1987SE

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Questions and answers

When was Laser Gas Mixtures cleared by the FDA?

Laser Gas Mixtures (K820535) received a 510(k) decision of Substantially Equivalent on March 31, 1982, 29 days after the submission was received.

What is the product code of K820535?

The FDA product code is EWG – Laser, Ent Microsurgical Carbon-Dioxide, a Class II (moderate risk) device regulated under 21 CFR 874.4500.