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)

BNOS MICROVENT, MODEL AC AND MODEL AO

K-Number: K944397 · 1995-01-31

Decision Date1995-01-31
Product CodeBTL
Advisory CommitteeAN
DecisionUnknown

Device Summary

BNOS MICROVENT, MODEL AC AND MODEL AO is the device name listed in this FDA 510(k) record. The listed applicant is Racal Health & Safety, Inc.. It received FDA 510(k) clearance on 1995-01-31 under 510(k) number K944397. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BNOS MICROVENT, MODEL AC AND MODEL AO?

BNOS MICROVENT, MODEL AC AND MODEL AO is a medical device that received FDA 510(k) clearance on 1995-01-31. The listed applicant is Racal Health & Safety, Inc.. The 510(k) number is K944397.

When did BNOS MICROVENT, MODEL AC AND MODEL AO receive FDA 510(k) clearance?

BNOS MICROVENT, MODEL AC AND MODEL AO received FDA 510(k) clearance on 1995-01-31, under 510(k) number K944397.

Who is the listed applicant for BNOS MICROVENT, MODEL AC AND MODEL AO?

The FDA 510(k) record lists Racal Health & Safety, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BNOS MICROVENT, MODEL AC AND MODEL AO?

The FDA product code for BNOS MICROVENT, MODEL AC AND MODEL AO is BTL.

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 Racal Health & Safety, 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.

Related Devices (Code: BTL)

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.

↑