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FDA 510(k)

OHMEDA 5410 VOLUME MONITOR

K-Number: K862687 · 1986-09-12

ApplicantOhmeda Medical
Decision Date1986-09-12
Product CodeBZK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHMEDA 5410 VOLUME MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1986-09-12 under 510(k) number K862687. The device is classified under product code BZK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMEDA 5410 VOLUME MONITOR?

OHMEDA 5410 VOLUME MONITOR is a medical device that received FDA 510(k) clearance on 1986-09-12. The listed applicant is Ohmeda Medical. The 510(k) number is K862687.

When did OHMEDA 5410 VOLUME MONITOR receive FDA 510(k) clearance?

OHMEDA 5410 VOLUME MONITOR received FDA 510(k) clearance on 1986-09-12, under 510(k) number K862687.

Who is the listed applicant for OHMEDA 5410 VOLUME MONITOR?

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

What is the FDA product code for OHMEDA 5410 VOLUME MONITOR?

The FDA product code for OHMEDA 5410 VOLUME MONITOR is BZK.

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Other records listing Ohmeda Medical as applicant

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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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