Who is the manufacturer of 3M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 8670?

3M Company filed the 510(k) submission for 3M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 8670 (K935304).

What is the FDA product code for 3M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 8670?

LWM. as a Class U device in the DE panel.

What is the regulatory pathway for 3M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 8670?

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

Who can help prepare an FDA 510(k) submission like 3M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 8670?

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.

3M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 8670

K935304 · 3M Company · LWM · Mar 16, 1994 · DE

Device Facts

Record ID	K935304
Device Name	3M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 8670
Applicant	3M Company
Product Code	LWM · DE
Decision Date	Mar 16, 1994
Decision	SESE
Submission Type	Traditional
Device Class	Class U

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