Question 1

Who is the manufacturer of MULTI-AD FLUID DISPENSING SYSTEM?

Accepted Answer

National Patent Development Corp. filed the 510(k) submission for MULTI-AD FLUID DISPENSING SYSTEM (K792227).

Question 2

What is the FDA product code for MULTI-AD FLUID DISPENSING SYSTEM?

Accepted Answer

KYX. It is classified under 21 CFR 880.6430 as a Class 1 device in the General Hospital panel.

Question 3

When was MULTI-AD FLUID DISPENSING SYSTEM cleared by the FDA?

Accepted Answer

Dec 20, 1979 (decision: SESE).

Question 4

What is the regulatory pathway for MULTI-AD FLUID DISPENSING SYSTEM?

Accepted Answer

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

Question 5

Who can help prepare an FDA 510(k) submission like MULTI-AD FLUID DISPENSING SYSTEM?

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	K792227
Device Name	MULTI-AD FLUID DISPENSING SYSTEM
Applicant	National Patent Development Corp.
Product Code	KYX · General Hospital
Decision Date	Dec 20, 1979
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 880.6430
Device Class	Class 1

MULTI-AD FLUID DISPENSING SYSTEM

Device Facts

Regulatory Classification

Identification