Conphar Airways

FDA 510(k) K791799 · Conphar, Inc.

Substantially Equivalent

510(k) numberK791799

Submission

Device name
Conphar Airways
Applicant
Conphar, Inc.
Mchenry, IL, US
Received
September 13, 1979
Decision date
September 19, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CAE – Airway, Oropharyngeal, Anesthesiology
Device class
Class I (low risk)
Regulation
21 CFR 868.5110
Specialty
Anesthesiology

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Questions and answers

When was Conphar Airways cleared by the FDA?

Conphar Airways (K791799) received a 510(k) decision of Substantially Equivalent on September 19, 1979, 6 days after the submission was received.

What is the product code of K791799?

The FDA product code is CAE – Airway, Oropharyngeal, Anesthesiology, a Class I (low risk) device regulated under 21 CFR 868.5110.