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FDA 510(k)

RICO RESPIRATION MONITOR

K-Number: K840975 · 1984-03-30

ApplicantJ.M. Laboratories, Inc.
Decision Date1984-03-30
Product CodeBZK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RICO RESPIRATION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is J.M. Laboratories, Inc.. It received FDA 510(k) clearance on 1984-03-30 under 510(k) number K840975. 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 RICO RESPIRATION MONITOR?

RICO RESPIRATION MONITOR is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is J.M. Laboratories, Inc.. The 510(k) number is K840975.

When did RICO RESPIRATION MONITOR receive FDA 510(k) clearance?

RICO RESPIRATION MONITOR received FDA 510(k) clearance on 1984-03-30, under 510(k) number K840975.

Who is the listed applicant for RICO RESPIRATION MONITOR?

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

What is the FDA product code for RICO RESPIRATION MONITOR?

The FDA product code for RICO RESPIRATION MONITOR is BZK.

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Related Devices (Code: BZK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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