Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PEDIATRIC VENTILATOR AND PARTNER VOLUME MONITOR

K-Number: K915488 · 1992-10-22

Decision Date1992-10-22
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC VENTILATOR AND PARTNER VOLUME MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Bird Products Corp.. It received FDA 510(k) clearance on 1992-10-22 under 510(k) number K915488. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC VENTILATOR AND PARTNER VOLUME MONITOR?

PEDIATRIC VENTILATOR AND PARTNER VOLUME MONITOR is a medical device that received FDA 510(k) clearance on 1992-10-22. The listed applicant is Bird Products Corp.. The 510(k) number is K915488.

When did PEDIATRIC VENTILATOR AND PARTNER VOLUME MONITOR receive FDA 510(k) clearance?

PEDIATRIC VENTILATOR AND PARTNER VOLUME MONITOR received FDA 510(k) clearance on 1992-10-22, under 510(k) number K915488.

Who is the listed applicant for PEDIATRIC VENTILATOR AND PARTNER VOLUME MONITOR?

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

What is the FDA product code for PEDIATRIC VENTILATOR AND PARTNER VOLUME MONITOR?

The FDA product code for PEDIATRIC VENTILATOR AND PARTNER VOLUME MONITOR is CBK.

Related Clinical Trials

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.

Other records listing Bird Products Corp. as applicant

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.

View all 35 devices →

Related Devices (Code: CBK)

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.

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.

↑