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FDA 510(k)

R-BAND(TM) RESPIRATORY SENSOR

K-Number: K900264 · 1990-07-24

ApplicantBuckman Co., Inc.
Decision Date1990-07-24
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

R-BAND(TM) RESPIRATORY SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1990-07-24 under 510(k) number K900264. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R-BAND(TM) RESPIRATORY SENSOR?

R-BAND(TM) RESPIRATORY SENSOR is a medical device that received FDA 510(k) clearance on 1990-07-24. The listed applicant is Buckman Co., Inc.. The 510(k) number is K900264.

When did R-BAND(TM) RESPIRATORY SENSOR receive FDA 510(k) clearance?

R-BAND(TM) RESPIRATORY SENSOR received FDA 510(k) clearance on 1990-07-24, under 510(k) number K900264.

Who is the listed applicant for R-BAND(TM) RESPIRATORY SENSOR?

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

What is the FDA product code for R-BAND(TM) RESPIRATORY SENSOR?

The FDA product code for R-BAND(TM) RESPIRATORY SENSOR is BZQ.

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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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