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)

MOFIFICATION BEAR NVM-1 NEONATAL VOLUME MONITOR

K-Number: K890724 · 1989-03-30

Decision Date1989-03-30
Product CodeBZK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MOFIFICATION BEAR NVM-1 NEONATAL VOLUME MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Bear Medical Systems, Inc.. It received FDA 510(k) clearance on 1989-03-30 under 510(k) number K890724. 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 MOFIFICATION BEAR NVM-1 NEONATAL VOLUME MONITOR?

MOFIFICATION BEAR NVM-1 NEONATAL VOLUME MONITOR is a medical device that received FDA 510(k) clearance on 1989-03-30. The listed applicant is Bear Medical Systems, Inc.. The 510(k) number is K890724.

When did MOFIFICATION BEAR NVM-1 NEONATAL VOLUME MONITOR receive FDA 510(k) clearance?

MOFIFICATION BEAR NVM-1 NEONATAL VOLUME MONITOR received FDA 510(k) clearance on 1989-03-30, under 510(k) number K890724.

Who is the listed applicant for MOFIFICATION BEAR NVM-1 NEONATAL VOLUME MONITOR?

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

What is the FDA product code for MOFIFICATION BEAR NVM-1 NEONATAL VOLUME MONITOR?

The FDA product code for MOFIFICATION BEAR NVM-1 NEONATAL 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 Bear Medical Systems, Inc. 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 28 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.

↑