Vital Statistics System (O-Cath Accessory)

FDA 510(k) K964978 · Quinton, Inc.

Substantially Equivalent

510(k) numberK964978

Submission

Device name
Vital Statistics System (O-Cath Accessory)
Applicant
Quinton, Inc.
Bothell, WA, US
Received
December 12, 1996
Decision date
May 21, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DQA – Oximeter
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2700
Specialty
Cardiovascular

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Questions and answers

When was Vital Statistics System (O-Cath Accessory) cleared by the FDA?

Vital Statistics System (O-Cath Accessory) (K964978) received a 510(k) decision of Substantially Equivalent on May 21, 1997, 160 days after the submission was received.

What is the product code of K964978?

The FDA product code is DQA – Oximeter, a Class II (moderate risk) device regulated under 21 CFR 870.2700.