Spirometer Isolation Valve #8890

FDA 510(k) K833088 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK833088

Submission

Device name
Spirometer Isolation Valve #8890
Applicant
Boehringer Mannheim Corp.
Mchenry, IL, US
Received
September 12, 1983
Decision date
October 28, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

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K952019Prima Adult Gas Sampling CircuitsCAI · Traditional Prima, Inc.05/22/1995SE
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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

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Questions and answers

When was Spirometer Isolation Valve #8890 cleared by the FDA?

Spirometer Isolation Valve #8890 (K833088) received a 510(k) decision of Substantially Equivalent on October 28, 1983, 46 days after the submission was received.

What is the product code of K833088?

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.