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FDA 510(k)

OXYGEN CONSUMPTION MONITOR #OCM-0100

K-Number: K823359 · 1983-01-05

ApplicantBentley Laboratories, Inc.
Decision Date1983-01-05
Product CodeDRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OXYGEN CONSUMPTION MONITOR #OCM-0100 is the device name listed in this FDA 510(k) record. The listed applicant is Bentley Laboratories, Inc.. It received FDA 510(k) clearance on 1983-01-05 under 510(k) number K823359. The device is classified under product code DRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXYGEN CONSUMPTION MONITOR #OCM-0100?

OXYGEN CONSUMPTION MONITOR #OCM-0100 is a medical device that received FDA 510(k) clearance on 1983-01-05. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K823359.

When did OXYGEN CONSUMPTION MONITOR #OCM-0100 receive FDA 510(k) clearance?

OXYGEN CONSUMPTION MONITOR #OCM-0100 received FDA 510(k) clearance on 1983-01-05, under 510(k) number K823359.

Who is the listed applicant for OXYGEN CONSUMPTION MONITOR #OCM-0100?

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

What is the FDA product code for OXYGEN CONSUMPTION MONITOR #OCM-0100?

The FDA product code for OXYGEN CONSUMPTION MONITOR #OCM-0100 is DRY.

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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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