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)

PARTNER VOLUME MONITOR

K-Number: K901885 · 1990-09-27

Decision Date1990-09-27
Product CodeBZK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

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 1990-09-27 under 510(k) number K901885. 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 PARTNER VOLUME MONITOR?

PARTNER VOLUME MONITOR is a medical device that received FDA 510(k) clearance on 1990-09-27. The listed applicant is Bird Products Corp.. The 510(k) number is K901885.

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

PARTNER VOLUME MONITOR received FDA 510(k) clearance on 1990-09-27, under 510(k) number K901885.

Who is the listed applicant for 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 PARTNER VOLUME MONITOR?

The FDA product code for PARTNER VOLUME MONITOR is BZK.

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: 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.

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.

↑