Question 1

Who is the manufacturer of EARSCAN?

Accepted Answer

Micro Audiometrics Corp. filed the 510(k) submission for EARSCAN (K812529).

Question 2

What is the FDA product code for EARSCAN?

Accepted Answer

EWO. It is classified under 21 CFR 874.1050 as a Class 2 device in the Ear, Nose, Throat panel.

Question 3

When was EARSCAN cleared by the FDA?

Accepted Answer

Oct 14, 1981 (decision: SESE).

Question 4

What is the regulatory pathway for EARSCAN?

Accepted Answer

510(k) clearance (submission type: Traditional).

Question 5

Who can help prepare an FDA 510(k) submission like EARSCAN?

Accepted Answer

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Record ID	K812529
Device Name	EARSCAN
Applicant	Micro Audiometrics Corp.
Product Code	EWO · Ear, Nose, Throat
Decision Date	Oct 14, 1981
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 874.1050
Device Class	Class 2

EARSCAN

Device Facts

Regulatory Classification

Identification