Low Dead Space Adaptor & Reuasable Airway Adaptor

Q: What is the product code of K930250?

The FDA product code is CCK – Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase, a Class II (moderate risk) device regulated under 21 CFR 868.1400.

FDA 510(k) K930250 · Pryon Corp.

Substantially Equivalent

510(k) numberK930250

Submission

Device name: Low Dead Space Adaptor & Reuasable Airway Adaptor
Applicant: Pryon Corp.
Menomonee Falls, WI, US
Received: January 6, 1993
Decision date: October 15, 1993
Decision: Substantially Equivalent (SESE)
Type: Traditional 510(k)
Summary: 510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code: CCK – Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Device class: Class II (moderate risk)
Regulation: 21 CFR 868.1400
Specialty: Anesthesiology

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K222511	Oxy2ProCCK · Traditional	Southmedic, Inc.	11/21/2023SE

More from Southmedic, Inc.

510(k)	Device	Decision
K942772	A-200 Multi-Use Airway AdapterCCK · Traditional	07/25/1994SE
K935272	Cap 400 atCCK · Traditional	07/13/1994SE
K915773	P-300 Capnograph and Pulse OximeterDQA · Traditional	06/24/1992SE

Questions and answers

When was Low Dead Space Adaptor & Reuasable Airway Adaptor cleared by the FDA?

Low Dead Space Adaptor & Reuasable Airway Adaptor (K930250) received a 510(k) decision of Substantially Equivalent on October 15, 1993, 282 days after the submission was received.

What is the product code of K930250?

The FDA product code is CCK – Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase, a Class II (moderate risk) device regulated under 21 CFR 868.1400.