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FDA 510(k)

ABG KITS - CMS 4000 SERIES

K-Number: K830333 · 1983-03-31

ApplicantCurrie Medical Specialties, Inc.
Decision Date1983-03-31
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ABG KITS - CMS 4000 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Currie Medical Specialties, Inc.. It received FDA 510(k) clearance on 1983-03-31 under 510(k) number K830333. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABG KITS - CMS 4000 SERIES?

ABG KITS - CMS 4000 SERIES is a medical device that received FDA 510(k) clearance on 1983-03-31. The listed applicant is Currie Medical Specialties, Inc.. The 510(k) number is K830333.

When did ABG KITS - CMS 4000 SERIES receive FDA 510(k) clearance?

ABG KITS - CMS 4000 SERIES received FDA 510(k) clearance on 1983-03-31, under 510(k) number K830333.

Who is the listed applicant for ABG KITS - CMS 4000 SERIES?

The FDA 510(k) record lists Currie Medical Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ABG KITS - CMS 4000 SERIES?

The FDA product code for ABG KITS - CMS 4000 SERIES is CBT.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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