Unicor, Inc. Gas Sampling Lines & Connectors

FDA 510(k) K953788 · Unicor, Inc.

Substantially Equivalent

510(k) numberK953788

Submission

Device name
Unicor, Inc. Gas Sampling Lines & Connectors
Applicant
Unicor, Inc.
Cleveland, TN, US
Received
August 14, 1995
Decision date
September 19, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CAI – Circuit, Breathing (W Connector, Adaptor, Y Piece)
Device class
Class I (low risk)
Regulation
21 CFR 868.5240
Specialty
Anesthesiology

Other 510(k)s with product code CAI

510(k)DeviceApplicantDecision
K954480Condensate Collection KitCAI · Traditional Nova-Ventrx12/29/1995SE
K953787Unicor, Inc. Adult Anesthesia Breathing CircuitCAI · Traditional Unicor, Inc.09/19/1995SE
K952020Prima Pediatric Anesthesia CircuitsCAI · Traditional Prima, Inc.05/22/1995SE
K952019Prima Adult Gas Sampling CircuitsCAI · Traditional Prima, Inc.05/22/1995SE
K952018Prima Coaxial CircuitsCAI · Traditional Prima, Inc.05/22/1995SE
K952017Prima Mapleson D CircuitCAI · Traditional Prima, Inc.05/22/1995SE
K952016Prima Pediatric Gas Sampling CircuitsCAI · Traditional Prima, Inc.05/22/1995SE
K952014Prima Adult Temperature Monitoring Anesthesia CircuitsCAI · Traditional Prima, Inc.05/22/1995SE
K952009Prima Pediatric Temperature Monitoring CircuitsCAI · Traditional Prima, Inc.05/19/1995SE
K945565Spiro-FlexCAI · Traditional Inhalation Plastics01/13/1995SE

More from Inhalation Plastics

510(k)DeviceDecision
K953787Unicor, Inc. Adult Anesthesia Breathing CircuitCAI · Traditional 09/19/1995SE
K953786Unicor, Inc. Connectors & Airway ExtensionsBZA · Traditional 09/19/1995SE
K953784Unicor, Inc. Corrugated TubingBZO · Traditional 09/19/1995SE
K953785Unicor, Inc. Ventilator HosesBZO · Traditional 09/18/1995SE

Questions and answers

When was Unicor, Inc. Gas Sampling Lines & Connectors cleared by the FDA?

Unicor, Inc. Gas Sampling Lines & Connectors (K953788) received a 510(k) decision of Substantially Equivalent on September 19, 1995, 36 days after the submission was received.

What is the product code of K953788?

The FDA product code is CAI – Circuit, Breathing (W Connector, Adaptor, Y Piece), a Class I (low risk) device regulated under 21 CFR 868.5240.